FDA Inspection 1178325 — Analogic Corporation

Analogic Corporation — FEI 1220672

The FDA completed an inspection of Analogic Corporation on August 25, 2022 in Peabody, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 25, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Peabody, MA (United States)

Citations

IDCFRDescription
315921 CFR 820.184DHR content