FDA Inspection 1055685 — Ferrosan Medical Devices Sp. Z O. O.
The FDA completed an inspection of Ferrosan Medical Devices Sp. Z O. O. on May 10, 2018 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
- May 10, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Szczecin (Poland)