FDA Inspection 1034466 — Arcade Marketing Inc.

Arcade Marketing Inc. — FEI 3002986405

The FDA completed an inspection of Arcade Marketing Inc. on November 30, 2017 in Chattanooga, TN. 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
November 30, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chattanooga, TN (United States)

Citations

IDCFRDescription
136121 CFR 211.100(a)Absence of Written Procedures
363221 CFR 211.170(b)Annual visual exams of drug products