FDA Inspection 920454 — RH USA INC
The FDA completed an inspection of RH USA INC on Mar 27, 2015 in Livermore, 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
- Mar 27, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Livermore, CA (United States)