FDA Inspection 837941 — Medi-Fare Drug

Medi-Fare Drug — FEI 3009925820

The FDA completed an inspection of Medi-Fare Drug on June 21, 2013 in Blacksburg, SC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 21, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Blacksburg, SC (United States)

Citations

IDCFRDescription
115921 CFR 211.28(a)Clothing appropriate for duties performed
119421 CFR 211.42(c)Defined areas of adequate size for operations
145121 CFR 211.113(b)Procedures for sterile drug products