FDA Inspection 1114052 — CCRM DFW

CCRM DFW — FEI 3008234883

The FDA completed an inspection of CCRM DFW on Dec 4, 2019 in Frisco, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 4, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Frisco, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.