FDA Inspection 1247485 — Klockner Of North America

Klockner Of North America — FEI 3011395139

The FDA completed an inspection of Klockner Of North America on Aug 21, 2024 in Miami, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 21, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Miami, FL (United States)