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FDA Inspection
•Beckman Coulter, Inc.•March 11, 2015

Beckman Coulter, Inc. – FDA Inspection, Mar 11, 2015

Record Details

This FDA Inspection record concerns Beckman Coulter, Inc., with an inspection on March 11, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
Beckman Coulter, Inc.
Inspection Date
March 11, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 21cbfedd-d98e-4a9d-bded-e8a9bf79ee85

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
918716
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 806.10(a)(1)Report of risk to health

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Beckman Coulter, Inc.

3
DateClassificationOfficeProject area
October 19, 2018Not classifiedSan Francisco District Office
January 24, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
July 3, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Beckman Coulter, Inc.
  • FDA Inspection 1110695 - 2018-10-19
  • FDA Inspection 864637 - 2014-01-24
  • FDA Inspection 791710 - 2012-07-03

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