FDA Inspection 943948 — Ferrosan Medical Devices Sp. Z O. O.
The FDA completed an inspection of Ferrosan Medical Devices Sp. Z O. O. on Sep 9, 2015 in Szczecin. 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
- Sep 9, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Szczecin (Poland)