FDA Inspection 1178689 — ITG-Medev, Inc.

ITG-Medev, Inc. — FEI 1000307251

The FDA completed an inspection of ITG-Medev, Inc. on August 16, 2022 in San Francisco, CA. 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
August 16, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Francisco, CA (United States)