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FDA Inspection 895141 — Analogic Corporation

Analogic Corporation — FEI 1220672

The FDA completed an inspection of Analogic Corporation on September 4, 2014 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
September 4, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Peabody, MA (United States)

Facility

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FDA data resources