FDA Inspection 826684 — Organon Pharma (UK) Ltd.

Organon Pharma (UK) Ltd. — FEI 3002807653

The FDA completed an inspection of Organon Pharma (UK) Ltd. on Mar 22, 2013 in Cramlington. 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 22, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cramlington (United Kingdom)

Citations

IDCFRDescription
135821 CFR 211.100(b)SOPs not followed / documented

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