FDA Inspection 993016 — Bauerfeind AG
The FDA completed an inspection of Bauerfeind AG on Nov 4, 2016 in Zeulenroda-Triebes. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 4, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Zeulenroda-Triebes (Germany)