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FDA Inspection 1011463 — Analogic Corporation

Analogic Corporation — FEI 1220672

The FDA completed an inspection of Analogic Corporation on May 17, 2017 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
May 17, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Peabody, MA (United States)

Facility

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FDA data resources