FDA inspection
Pfizer Pharmaceutical Llc.: FDA inspection ending May 26, 2005
FDA inspection 384445 · Voluntary Action Indicated (VAI) · Barceloneta, PR
Key facts
| Inspection ID | 384445 |
|---|---|
| Firm | Pfizer Pharmaceutical Llc. |
| FEI number | 2650011 |
| Address | Hwy #2 Rd 140 Km 64.4 |
| City | Barceloneta |
| State | PR |
| ZIP | 00617 |
| Fiscal year | 2005 |
| Inspection end date | May 26, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| 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|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation|New Drug Evaluation|OTC Drug Evaluation |
| Product type | Drugs |
At a glance
- None 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