FDA Inspection 1091323 — Colgate-Palmolive Company

Colgate-Palmolive Company — FEI 2221095

The FDA completed an inspection of Colgate-Palmolive Company on May 30, 2019 in Piscataway, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 30, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Piscataway, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Citations

IDCFRDescription
8936FDCA 760(b)(1)No label copy submitted with AE report (non-Rx drug)