FDA Inspection 854326 — Dr. Brown's Company

Dr. Brown's Company — FEI 3008819945

The FDA completed an inspection of Dr. Brown's Company on Oct 31, 2013 in Bonne Terre, MO. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 31, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Bonne Terre, MO (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained