FDA Inspection 1080883 — BECTON, DICKINSON & CO., (BD)

BECTON, DICKINSON & CO., (BD) — FEI 1024879

The FDA completed an inspection of BECTON, DICKINSON & CO., (BD) on Mar 1, 2019 in Sumter, SC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 1, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Sumter, SC (United States)

Citations

IDCFRDescription
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures