FDA Inspection 764802 — Angiodynamics Inc

Angiodynamics Inc — FEI 1000523114

The FDA completed an inspection of Angiodynamics Inc on February 13, 2012 in Marlborough, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 13, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Marlborough, MA (United States)

Citations

IDCFRDescription
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
310421 CFR 820.30(j)Design history file
313021 CFR 820.100(a)Lack of or inadequate procedures
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
383721 CFR 820.25(b)Training records