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FDA Inspection 951698 — Johnson & Johnson Consumer Inc

Johnson & Johnson Consumer Inc — FEI 2010632

The FDA completed an inspection of Johnson & Johnson Consumer Inc on October 8, 2015 in Los Angeles, CA. 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
October 8, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Los Angeles, CA (United States)

Facility

Other inspections at this facility

  • 1122793 (NAI Wed Mar 11 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 832129 (NAI Thu May 16 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 679108 (VAI Thu Aug 12 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources