FDA Inspection 600262 — Reckitt Benckiser (UK) Ltd.

Reckitt Benckiser (UK) Ltd. — FEI 3002807985

The FDA completed an inspection of Reckitt Benckiser (UK) Ltd. on July 22, 2009 in Hull. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 22, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hull (United Kingdom)