FDA Inspection 1029403 — RH USA INC
The FDA completed an inspection of RH USA INC on Oct 12, 2017 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
- Oct 12, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Livermore, CA (United States)