FDA inspection
Precision Medical Devices Inc.: FDA inspection ending Mar 12, 2019
FDA inspection 1082296 · Voluntary Action Indicated (VAI) · New Brunswick, NJ
Key facts
| Inspection ID | 1082296 |
|---|---|
| Firm | Precision Medical Devices Inc. |
| FEI number | 3007478714 |
| Address | 121 Jersey Ave Ste 203 |
| City | New Brunswick |
| State | NJ |
| ZIP | 08901 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Mar 12, 2019 |
| 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