FDA Inspection 1248564 — N.V. Organon

N.V. Organon — FEI 3002806821

The FDA completed an inspection of N.V. Organon on Sep 8, 2022 in Oss. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 8, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oss (Netherlands)

Additional details

Mutual Recognition Agreement (MRA)

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