FDA Inspection 1010212 — Delille Oxygen Company

Delille Oxygen Company — FEI 1513845

The FDA completed an inspection of Delille Oxygen Company on April 12, 2017 in Columbus, OH. 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
April 12, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Columbus, OH (United States)

Citations

IDCFRDescription
356921 CFR 211.89Quarantine of Rejected Components et. al.