FDA inspection
Propper Mfg Co Inc: FDA inspection ending Sep 14, 2021
FDA inspection 1152179 · No Action Indicated (NAI) · Long Island City, NY
Key facts
| Inspection ID | 1152179 |
|---|---|
| Firm | Propper Mfg Co Inc |
| FEI number | 2410251 |
| Address | 3604 Skillman Ave |
| City | Long Island City |
| State | NY |
| ZIP | 11101 |
| Country | United States |
| Fiscal year | 2021 |
| Inspection end date | Sep 14, 2021 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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