FDA Inspection 1019862 — TreyMed, Inc.
The FDA completed an inspection of TreyMed, Inc. on Jul 12, 2017 in Sussex, WI. 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
- Jul 12, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sussex, WI (United States)