FDA Inspection 1101763 — ATEK Manufacturing
The FDA completed an inspection of ATEK Manufacturing on July 2, 2019 in Brainerd, 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
- July 2, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Brainerd, MN (United States)