FDA Inspection 918166 — Ameritek USA, Inc.
The FDA completed an inspection of Ameritek USA, Inc. on March 12, 2015 in Everett, WA. 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
- March 12, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Everett, WA (United States)