FDA Inspection 1096402 — Eurofins Biopharma Product Testing Munich GmbH
The FDA completed an inspection of Eurofins Biopharma Product Testing Munich GmbH on July 12, 2019 in Planegg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 12, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Planegg (Germany)
Citations
| ID | CFR | Description |
|---|---|---|
| 2401 | 21 CFR 211.194(a)(4) | Complete Test Data |