FDA Inspection 1155767 — ITG-Medev, Inc.

ITG-Medev, Inc. — FEI 1000307251

The FDA completed an inspection of ITG-Medev, Inc. on October 22, 2021 in San Francisco, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 22, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
San Francisco, CA (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation
369621 CFR 820.100(b)Documentation