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FDA Inspection 1109873 — Analogic Corporation

Analogic Corporation — FEI 1220672

The FDA completed an inspection of Analogic Corporation on November 4, 2019 in Peabody, MA. 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
November 4, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Peabody, MA (United States)

Facility

Other inspections at this facility

  • 1178325 (VAI Thu Aug 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1011463 (NAI Wed May 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 895141 (NAI Thu Sep 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 773986 (NAI Fri Mar 23 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 745355 (NAI Mon Sep 19 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources