FDA Inspection 910481 — I-Tek Medical Inc
The FDA completed an inspection of I-Tek Medical Inc on November 20, 2014 in White Bear Lake, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 20, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- White Bear Lake, MN (United States)