FDA Inspection 1310330 — Pausch Medical GmbH
The FDA completed an inspection of Pausch Medical GmbH on April 1, 2026 in Erlangen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- April 1, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Erlangen (Germany)
Citations
| ID | CFR | Description |
|---|---|---|
| 5700 | 21 CFR 1002.10 | Failure to submit, distinct marking |