FDA inspection
Pepin Manufacturing Inc: FDA inspection ending May 27, 2008
FDA inspection 522962 · No Action Indicated (NAI) · Lake City, MN
Key facts
| Inspection ID | 522962 |
|---|---|
| Firm | Pepin Manufacturing Inc |
| FEI number | 1000221051 |
| Address | 1875 S Highway 61 |
| City | Lake City |
| State | MN |
| ZIP | 55041-9556 |
| Fiscal year | 2008 |
| Inspection end date | May 27, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
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