FDA Inspection 795199 — Ormco Corporation
The FDA completed an inspection of Ormco Corporation on Aug 10, 2012 in Pomona, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 10, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Pomona, CA (United States)