FDA Inspection 912585 — ARMM Inc
The FDA completed an inspection of ARMM Inc on February 4, 2015 in Huntington Beach, CA. 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
- February 4, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Huntington Beach, CA (United States)