FDA inspection
Procter & Gamble Manufacturing GmbH: FDA inspection ending Jul 24, 2015
FDA inspection 940338 · Voluntary Action Indicated (VAI) · Gros-Gerau
Key facts
| Inspection ID | 940338 |
|---|---|
| Firm | Procter & Gamble Manufacturing GmbH |
| FEI number | 3001903296 |
| Address | Procter-und-Gamble-Str. 1 |
| City | Gros-Gerau |
| Country | Germany |
| Fiscal year | 2015 |
| Inspection end date | Jul 24, 2015 |
| 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
- 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