FDA Inspection 848116 — Johnson & Johnson Consumer, Inc

Johnson & Johnson Consumer, Inc — FEI 1000150647

The FDA completed an inspection of Johnson & Johnson Consumer, Inc on August 30, 2013 in Lancaster, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 30, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lancaster, PA (United States)

Citations

IDCFRDescription
117721 CFR 211.63Equipment Design, Size and Location
202721 CFR 211.192Investigations of discrepancies, failures