FDA Inspection 1024610 — Arm Medical Devices, Inc.
The FDA completed an inspection of Arm Medical Devices, Inc. on September 7, 2017 in Bristol, CT. 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
- September 7, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Bristol, CT (United States)