FDA Inspection 796648 — In VitroTech Labs, Inc.

In VitroTech Labs, Inc. — FEI 3008771840

The FDA completed an inspection of In VitroTech Labs, Inc. on Aug 16, 2012 in West Hollywood, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 16, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
West Hollywood, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.