FDA inspection
Carroll-Baccari, Inc.: FDA inspection ending Sep 2, 2005
FDA inspection 396920 · Voluntary Action Indicated (VAI) · Riviera Beach, FL
Key facts
| Inspection ID | 396920 |
|---|---|
| Firm | Carroll-Baccari, Inc. |
| FEI number | 3000296486 |
| Address | 6625 White Dr |
| City | Riviera Beach |
| State | FL |
| ZIP | 33407-1209 |
| Fiscal year | 2005 |
| Inspection end date | Sep 2, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug 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Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs|Drug Quality Assurance|Postmarket Assurance: Med Devices|Unapproved and Misbranded Drugs |
| Product type | Devices, Drugs |
At a glance
- 10–99 Citations
- 1–9 Posted citations
- No 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