FDA Inspection 1043733 — Rotation Medical, Inc.
The FDA completed an inspection of Rotation Medical, Inc. on Dec 20, 2017 in Plymouth, MN. 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
- Dec 20, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Plymouth, MN (United States)