FDA Inspection 730304 — Johnson & Johnson Vision Care, Inc.

Johnson & Johnson Vision Care, Inc. — FEI 1000222023

The FDA completed an inspection of Johnson & Johnson Vision Care, Inc. on June 17, 2011 in Jacksonville, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 17, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1471621 CFR 820.30(f)Design verification - output does not meet input requirement
333121 CFR 820.181DMR - not or inadequately maintained
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures