FDA inspection
MEDA Manufacturing GmbH: FDA inspection ending Sep 7, 2017
FDA inspection 1024520 · Voluntary Action Indicated (VAI) · Cologne
Key facts
| Inspection ID | 1024520 |
|---|---|
| Firm | MEDA Manufacturing GmbH |
| FEI number | 3002808393 |
| Address | Neurather Ring 1 |
| City | Cologne |
| Country | Germany |
| Fiscal year | 2017 |
| Inspection end date | Sep 7, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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