FDA Inspection 1021664 — Bullet Line LLC

Bullet Line LLC — FEI 3005625923

The FDA completed an inspection of Bullet Line LLC on August 15, 2017 in Florence, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 15, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Florence, KY (United States)

Citations

IDCFRDescription
150421 CFR 211.122(d)Labels and labeling stored separately
201121 CFR 211.188(a)Accurate reproduction