FDA Inspection 1172707 — Euromed, Inc.

Euromed, Inc. — FEI 3000719502

The FDA completed an inspection of Euromed, Inc. on June 10, 2022 in Orangeburg, NY. 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
June 10, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Orangeburg, NY (United States)