FDA Inspection 749823 — BJC Home Medical Equip

BJC Home Medical Equip — FEI 1000118291

The FDA completed an inspection of BJC Home Medical Equip on Oct 7, 2011 in Saint Louis, 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 7, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)

Citations

IDCFRDescription
136121 CFR 211.100(a)Absence of Written Procedures