FDA Inspection 833469 — Coupler LLC

Coupler LLC — FEI 3003734940

The FDA completed an inspection of Coupler LLC on May 29, 2013 in West Chester, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 29, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Chester, PA (United States)

Citations

IDCFRDescription
117721 CFR 211.63Equipment Design, Size and Location
121521 CFR 211.67(b)Written procedures not established/followed
357021 CFR 211.100(a)Approval and review of procedures
357121 CFR 211.100(a)Changes to Procedures Not Reviewed, Approved