FDA Inspection 715418 — Trividia Manufacturing Solutions, Inc.

Trividia Manufacturing Solutions, Inc. — FEI 1210279

The FDA completed an inspection of Trividia Manufacturing Solutions, Inc. on March 2, 2011 in Lancaster, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 2, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Lancaster, NH (United States)

Citations

IDCFRDescription
440021 CFR 211.186(b)(8)Description of containers, labels, et. al.