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FDA Inspection
•Becton Dickinson Medical Systems•March 16, 2012

Becton Dickinson Medical Systems – FDA Inspection, Mar 16, 2012

Record Details

This FDA Inspection record concerns Becton Dickinson Medical Systems, with an inspection on March 16, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
Becton Dickinson Medical Systems
Inspection Date
March 16, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · f39b0317-75fd-4a67-bca3-1f5c242f23ac

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
773046
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 803.50(a)(2)Individual Report of Malfunction
  2. 21 CFR 820.80(c)Lack of or inadequate In-process acceptance procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Becton Dickinson Medical Systems

4
DateClassificationOfficeProject area
September 15, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 2, 2017NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 23, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 15, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Becton Dickinson Medical Systems
  • FDA Inspection 1218321 - 2023-09-15
  • FDA Inspection 1021013 - 2017-08-02
  • FDA Inspection 912140 - 2015-01-23
  • FDA Inspection 823601 - 2013-03-15

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