FDA Inspection 1180897 — TreyMed, Inc.

TreyMed, Inc. — FEI 3003007937

The FDA completed an inspection of TreyMed, Inc. on September 16, 2022 in Sussex, WI. 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 16, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Sussex, WI (United States)