FDA Inspection 600262 — Reckitt Benckiser (UK) Ltd.

Reckitt Benckiser (UK) Ltd. — FEI 3002807985

The FDA completed an inspection of Reckitt Benckiser (UK) Ltd. on Jul 22, 2009 in Hull. 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
Jul 22, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hull (United Kingdom)

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