FDA Inspection 886119 — Scanfil Atvidaberg AB
The FDA completed an inspection of Scanfil Atvidaberg AB on Jul 3, 2014 in Atvidaberg. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 3, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Atvidaberg (Sweden)