FDA Inspection 791803 — Ultratellege USA Co. Ltd.
The FDA completed an inspection of Ultratellege USA Co. Ltd. on July 18, 2012 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
- July 18, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Erie, PA (United States)