FDA Inspection 649295 — Analogic Corporation

Analogic Corporation — FEI 1220672

The FDA completed an inspection of Analogic Corporation on February 16, 2010 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
February 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Peabody, MA (United States)