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FDA Inspection 1148296 — KLEB Inc

KLEB Inc — FEI 3013157033

The FDA completed an inspection of KLEB Inc on July 28, 2021 in Louisville, KY. 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 28, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Louisville, KY (United States)

Facility

Other inspections at this facility

  • 1216491 (NAI Thu Aug 24 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1040736 (NAI Wed Feb 07 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 957586 (NAI Wed Feb 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 837858 (NAI Tue Jun 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 631306 (NAI Wed Dec 02 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources