FDA Inspection 1045087 — In VitroTech Labs, Inc.

In VitroTech Labs, Inc. — FEI 3008771840

The FDA completed an inspection of In VitroTech Labs, Inc. on Mar 21, 2018 in West Hollywood, 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 21, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
West Hollywood, CA (United States)

Citations

IDCFRDescription
1223721 CFR 1271.55(a)(3)Summary--records used to make determination

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