FDA Inspection 849005 — MVF LLC

MVF LLC — FEI 3003941306

The FDA completed an inspection of MVF LLC on September 12, 2013 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
September 12, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Scottsdale, AZ (United States)