FDA Inspection 978123 — AliMed Corporation

AliMed Corporation — FEI 1218386

The FDA completed an inspection of AliMed Corporation on July 7, 2016 in Dedham, 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
July 7, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Dedham, MA (United States)

Citations

IDCFRDescription
41921 CFR 820.20(b)Lack of or inadequate organizational structure