FDA Inspection 1241212 — VFX Laboratories LLC

VFX Laboratories LLC — FEI 3030377014

The FDA completed an inspection of VFX Laboratories LLC on Jun 11, 2024 in Grapevine, TX. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 11, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Grapevine, TX (United States)

Citations

IDCFRDescription
136121 CFR 211.100(a)Absence of Written Procedures
183321 CFR 211.84(d)(1)Identity Testing of Each Component