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FDA Inspection 1119118 — Goetze-Niemer Co Inc

Goetze-Niemer Co Inc — FEI 3002177077

The FDA completed an inspection of Goetze-Niemer Co Inc on February 5, 2020 in Kansas City, MO. 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
February 5, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Kansas City, MO (United States)

Facility

Other inspections at this facility

  • 1044414 (NAI Thu Mar 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952168 (VAI Mon Dec 14 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 870748 (VAI Wed Mar 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources