FDA Inspection 853355 — Dr. Brown's Company

Dr. Brown's Company — FEI 3008138005

The FDA completed an inspection of Dr. Brown's Company on Oct 31, 2013 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 31, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Louis, MO (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures