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FDA Inspection 1256891 — Avery Biomedical Devices, Inc.

Avery Biomedical Devices, Inc. — FEI 2427696

The FDA completed an inspection of Avery Biomedical Devices, Inc. on October 30, 2024 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
October 30, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Commack, NY (United States)

Facility

Other inspections at this facility

  • 1167847 (NAI Thu Apr 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1096555 (VAI Tue Jul 16 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1008035 (VAI Mon Apr 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 972473 (NAI Thu Mar 24 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 819568 (NAI Wed Feb 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources