Beckman Coulter, Inc.

Form 483FOIA Uncovered

Chaska, MinnesotaFEI 2122870Issued December 11, 2023

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2122870.

ObservationsNot available

Issue DateDecember 11, 2023

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Beckman Coulter, Inc.
Location: Chaska, Minnesota
FEI Number: 2122870
Product Type: Devices
Issue Date: December 11, 2023
Country: United States

Inspection History, 2011 to 2025

NAI2

VAI2

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Beckman Coulter, Inc. FDA Form 483, Chaska, Minnesota, December 11, 2023