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FDA Inspection 1016290 — ClinImmune Labs

ClinImmune Labs — FEI 3000719146

The FDA completed an inspection of ClinImmune Labs on April 19, 2017 in Aurora, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 19, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Aurora, CO (United States)

Facility

Other inspections at this facility

  • 1220023 (NAI Tue Sep 19 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1098114 (VAI Fri Jul 19 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 858177 (NAI Wed Nov 27 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 825492 (VAI Thu Mar 28 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 701279 (NAI Fri Dec 10 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources