FDA Inspection 672612 — Refractec LLC
The FDA completed an inspection of Refractec LLC on Jun 17, 2010 in Bloomington, 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
- Jun 17, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bloomington, MN (United States)