FDA Inspection 1273172 — Organon Pharma (UK) Ltd.

Organon Pharma (UK) Ltd. — FEI 3002807653

The FDA completed an inspection of Organon Pharma (UK) Ltd. on June 13, 2025 in Cramlington. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 13, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cramlington (United Kingdom)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
121321 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
184321 CFR 211.84(d)(2)Component written specification