FDA Inspection 838938 — Bisico Bielefelder Dentalsilicone GmbH & Co. KG
The FDA completed an inspection of Bisico Bielefelder Dentalsilicone GmbH & Co. KG on Jun 20, 2013 in Bielefeld. 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
- Jun 20, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bielefeld (Germany)