FDA Inspection 1044414 — Goetze-Niemer Co Inc

Goetze-Niemer Co Inc — FEI 3002177077

The FDA completed an inspection of Goetze-Niemer Co Inc on March 8, 2018 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
March 8, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Kansas City, MO (United States)