FDA Inspection 873614 — N.V. Organon

N.V. Organon — FEI 3002806821

The FDA completed an inspection of N.V. Organon on Feb 7, 2014 in Oss. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 7, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oss (Netherlands)

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