FDA inspection
Catalent Germany Eberbach GmbH: FDA inspection ending Mar 18, 2016
FDA inspection 989834 · No Action Indicated (NAI) · Eberbach
Key facts
| Inspection ID | 989834 |
|---|---|
| Firm | Catalent Germany Eberbach GmbH |
| FEI number | 3002808098 |
| Address | Gammelsbacher Str. 2 |
| City | Eberbach |
| Country | Germany |
| Fiscal year | 2016 |
| Inspection end date | Mar 18, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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