FDA Inspection 1016495 — PhysioRX LLC

PhysioRX LLC — FEI 3010303196

The FDA completed an inspection of PhysioRX LLC on June 2, 2017 in Ocoee, FL. 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
June 2, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Ocoee, FL (United States)