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FDA Inspection 1260121 — MVF LLC

MVF LLC — FEI 3003941306

The FDA completed an inspection of MVF LLC on January 31, 2025 in Scottsdale, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 31, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Scottsdale, AZ (United States)

Facility

Other inspections at this facility

  • 1140539 (NAI Mon Apr 12 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1082772 (NAI Wed Mar 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1071568 (NAI Mon Oct 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 989326 (VAI Tue Jul 26 2016 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