FDA Inspection 1155767 — ITG-Medev, Inc.

ITG-Medev, Inc. — FEI 1000307251

The FDA completed an inspection of ITG-Medev, Inc. on Oct 22, 2021 in San Francisco, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 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

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