FDA inspection
Patheon API Manufacturing Inc: FDA inspection ending May 23, 2002
FDA inspection 216769 · Voluntary Action Indicated (VAI) · Greenville, SC
Key facts
| Inspection ID | 216769 |
|---|---|
| Firm | Patheon API Manufacturing Inc |
| FEI number | 3001451369 |
| Address | 309 Delaware St |
| City | Greenville |
| State | SC |
| ZIP | 29605-5420 |
| Fiscal year | 2002 |
| Inspection end date | May 23, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New 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