FDA Inspection 913244 — Reckitt Benckiser France

Reckitt Benckiser France — FEI 3003603433

The FDA completed an inspection of Reckitt Benckiser France on Jan 15, 2015 in Chartres. 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). 4 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 15, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chartres (France)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
144821 CFR 211.111Establishment of time limitations
360321 CFR 211.160(b)Scientifically sound laboratory controls
430521 CFR 211.68(b)Backup data not assured as exact and complete

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.