FDA Inspection 1098118 — Peramed Medizintechnik
The FDA completed an inspection of Peramed Medizintechnik on July 25, 2019 in Tuningen. 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
- July 25, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tuningen (Germany)
Citations
| ID | CFR | Description |
|---|---|---|
| 537 | 21 CFR 820.70(a) | Production processes |