FDA inspection
Propper Mfg Co Inc: FDA inspection ending Dec 21, 2017
FDA inspection 1035639 · Voluntary Action Indicated (VAI) · Long Island City, NY
Key facts
| Inspection ID | 1035639 |
|---|---|
| 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 | 2018 |
| Inspection end date | Dec 21, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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