FDA Inspection 979170 — Ultratellege USA Co. Ltd.
The FDA completed an inspection of Ultratellege USA Co. Ltd. on June 21, 2016 in Erie, PA. 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
- June 21, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Erie, PA (United States)