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FDA Inspection 989326 — MVF LLC

MVF LLC — FEI 3003941306

The FDA completed an inspection of MVF LLC on July 26, 2016 in Scottsdale, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 26, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Scottsdale, AZ (United States)

Facility

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  • 1071568 (NAI Mon Oct 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 970528 (NAI Wed Apr 27 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources