FDA inspection
Flawless Beauty and Skin: FDA inspection ending Jan 19, 2022
FDA inspection 1165296 · Official Action Indicated (OAI) · Ocean, NJ
Key facts
| Inspection ID | 1165296 |
|---|---|
| Firm | Flawless Beauty and Skin |
| FEI number | 3011055149 |
| Address | 1750 Brielle Ave Ste A3 A4 And A6 |
| City | Ocean |
| State | NJ |
| ZIP | 07712-3948 |
| Fiscal year | 2022 |
| Inspection end date | Jan 19, 2022 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Unapproved and Misbranded Drugs |
| Product type | Devices, Drugs |
| Warning letter | 630567 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data