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FDA Inspection 1028800 — CCRM Newport Beach Inc

CCRM Newport Beach Inc — FEI 3006397636

The FDA completed an inspection of CCRM Newport Beach Inc on September 28, 2017 in Newport Beach, CA. 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 28, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Newport Beach, CA (United States)

Facility

Other inspections at this facility

  • 1252488 (NAI Tue Oct 08 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1102754 (NAI Mon Jul 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 930809 (NAI Fri Jun 19 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 845765 (NAI Thu Aug 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 704356 (NAI Thu Jan 06 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources