FDA Inspection 706920 — MVF LLC

MVF LLC — FEI 3003941306

The FDA completed an inspection of MVF LLC on January 19, 2011 in Scottsdale, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 19, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Scottsdale, AZ (United States)

Citations

IDCFRDescription
1222121 CFR 1271.47(a)Procedures for all other requirements
1223821 CFR 1271.55(b)(1)Statement re: certified testing lab
1224021 CFR 1271.55(b)(3)Name and address on summary