FDA inspection
Primotec LLC: FDA inspection ending Sep 25, 2019
FDA inspection 1102929 · Voluntary Action Indicated (VAI) · Norwalk, CT
Key facts
| Inspection ID | 1102929 |
|---|---|
| Firm | Primotec LLC |
| FEI number | 3004491043 |
| Address | 360 Westport Ave |
| City | Norwalk |
| State | CT |
| ZIP | 06851 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Sep 25, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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