FDA Inspection 998804 — Mobius Bionics LLC
The FDA completed an inspection of Mobius Bionics LLC on January 26, 2017 in Manchester, NH. 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
- January 26, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Manchester, NH (United States)