FDA inspection
Catalent Pharma Solutions LLC: FDA inspection ending Jun 7, 2001
FDA inspection 76182 · Official Action Indicated (OAI) · Winchester, KY
Key facts
| Inspection ID | 76182 |
|---|---|
| Firm | Catalent Pharma Solutions LLC |
| FEI number | 1000122400 |
| Address | 1100 Enterprise Dr |
| City | Winchester |
| State | KY |
| ZIP | 40391-9668 |
| Fiscal year | 2001 |
| Inspection end date | Jun 7, 2001 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne 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Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation|Foodborne Biological Hazard|New Drug Evaluation |
| Product type | Drugs, Food/Cosmetics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 10–99 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