FDA Inspection 1026619 — Katena Products, Inc.

Katena Products, Inc. — FEI 2242450

The FDA completed an inspection of Katena Products, Inc. on September 12, 2017 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
September 12, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Randolph, NJ (United States)