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FDA Inspection 1114594 — Katena Products, Inc.

Katena Products, Inc. — FEI 2242450

The FDA completed an inspection of Katena Products, Inc. on January 6, 2020 in Randolph, NJ. 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
January 6, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Randolph, NJ (United States)

Facility

Other inspections at this facility

  • 1234623 (NAI Fri Mar 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1026619 (NAI Tue Sep 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 986240 (NAI Wed Aug 31 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768294 (NAI Wed Feb 22 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 629009 (VAI Mon Nov 09 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources