FDA Inspection 613585 — Sohniks
The FDA completed an inspection of Sohniks on Apr 27, 2009 in Eagan, MN. 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
- Apr 27, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Eagan, MN (United States)