FDA Inspection 1236262 — RH USA INC
The FDA completed an inspection of RH USA INC on Apr 10, 2024 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
- Apr 10, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Livermore, CA (United States)