FDA Inspection 659177 — ARMM Inc
The FDA completed an inspection of ARMM Inc on April 23, 2010 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
- April 23, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Huntington Beach, CA (United States)