FDA Inspection 863004 — Aba-Pgt Inc.

Aba-Pgt Inc. — FEI 3000171110

The FDA completed an inspection of Aba-Pgt Inc. on January 9, 2014 in Manchester, CT. 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
January 9, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Manchester, CT (United States)

Citations

IDCFRDescription
63021 CFR 803.17Lack of Written MDR Procedures