FDA Inspection 997754 — Uromedica Inc.
The FDA completed an inspection of Uromedica Inc. on Jan 11, 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
- Jan 11, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Plymouth, MN (United States)
Additional Details
Postmarket Audit Inspections