FDA Inspection 770613 — Airweld, Inc

Airweld, Inc — FEI 2432627

The FDA completed an inspection of Airweld, Inc on March 8, 2012 in Maspeth, NY. 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
March 8, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Maspeth, NY (United States)

Citations

IDCFRDescription
111221 CFR 211.25(a)Training--operations, GMPs, written procedures
113321 CFR 211.25(a)GMP Training Frequency