FDA inspection
Minakem Dunkerque Production: FDA inspection ending Apr 22, 2016
FDA inspection 975602 · Voluntary Action Indicated (VAI) · Dunkirk
Key facts
| Inspection ID | 975602 |
|---|---|
| Firm | Minakem Dunkerque Production |
| FEI number | 3008093605 |
| Address | Zone D Entreprises Du Nord Gracht |
| City | Dunkirk |
| Country | France |
| Fiscal year | 2016 |
| Inspection end date | Apr 22, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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