FDA inspection
Aaron Thomas Company Inc: FDA inspection ending Jul 24, 2003
FDA inspection 283543 · No Action Indicated (NAI) · Garden Grove, CA
Key facts
| Inspection ID | 283543 |
|---|---|
| Firm | Aaron Thomas Company Inc |
| FEI number | 2050161 |
| Address | 7421 Chapman Ave |
| City | Garden Grove |
| State | CA |
| ZIP | 92841-2115 |
| Fiscal year | 2003 |
| Inspection end date | Jul 24, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med 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Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard|Compliance: Med Devices|Drug Quality Assurance|Foodborne Biological Hazard |
| Product type | Devices, Drugs, Food/Cosmetics |
At a glance
- None Citations
- None 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