FDA inspection
K. W. Griffen Company DBA Biomed Packaging Systems: FDA inspection ending Jun 24, 2003
FDA inspection 280077 · No Action Indicated (NAI) · Norwalk, CT
Key facts
| Inspection ID | 280077 |
|---|---|
| Firm | K. W. Griffen Company DBA Biomed Packaging Systems |
| FEI number | 1211177 |
| Address | 100 Pearl St |
| City | Norwalk |
| State | CT |
| ZIP | 06850-1629 |
| Fiscal year | 2003 |
| Inspection end date | Jun 24, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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