FDA Inspection 908900 — Admedes GmbH
The FDA completed an inspection of Admedes GmbH on December 11, 2014 in Pforzheim. 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: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 11, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Pforzheim (Germany)
Citations
| ID | CFR | Description |
|---|---|---|
| 537 | 21 CFR 820.70(a) | Production processes |