FDA Inspection 972473 — Avery Biomedical Devices, Inc.

Avery Biomedical Devices, Inc. — FEI 2427696

The FDA completed an inspection of Avery Biomedical Devices, Inc. on March 24, 2016 in Commack, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 24, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Commack, NY (United States)