FDA Inspection 1024996 — Ultratellege USA Co. Ltd.
The FDA completed an inspection of Ultratellege USA Co. Ltd. on August 23, 2017 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
- August 23, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Erie, PA (United States)