FDA Inspection 882250 — Angiodynamics Inc

Angiodynamics Inc — FEI 1000523114

The FDA completed an inspection of Angiodynamics Inc on May 28, 2014 in Marlborough, MA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 28, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Marlborough, MA (United States)

Citations

IDCFRDescription
1471421 CFR 820.30(c)Design input - Lack of or inadequate procedures
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
265021 CFR 820.30(f)Design verification - Lack of or inadequate procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
320621 CFR 820.50(b)Approval, inadequate purchasing data
73221 CFR 803.50(a)(2)Individual Report of Malfunction