FDA Inspection 1023819 — CCRM DFW

CCRM DFW — FEI 3008234883

The FDA completed an inspection of CCRM DFW on July 25, 2017 in Frisco, TX. 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
July 25, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Frisco, TX (United States)