FDA Inspection 1028481 — Ancora Industries Inc

Ancora Industries Inc — FEI 3010023733

The FDA completed an inspection of Ancora Industries Inc on October 12, 2017 in Ronkonkoma, NY. 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
October 12, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Ronkonkoma, NY (United States)

Citations

IDCFRDescription
320321 CFR 820.40(b)Document change records, maintained.