FDA Inspection 762396 — Aesculap-Chifa SP. Z.O.O.
The FDA completed an inspection of Aesculap-Chifa SP. Z.O.O. on Dec 1, 2011 in Nowy Tomysl. 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
- Dec 1, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Nowy Tomysl (Poland)