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FDA Inspection
•Abbott GmbH•September 7, 2018

Abbott GmbH – FDA Inspection, Sep 7, 2018

Record Details

This FDA Inspection record concerns Abbott GmbH, with an inspection on September 7, 2018, issued by the Office of Inspections and Investigations, covering biologics.

Company
Abbott GmbH
Inspection Date
September 7, 2018
Product Type
Biologics
Office
Office of Inspections and Investigations
People
  • Krishnakum Devadas (Issuing Officer)
  • Nicole M. Li (Issuing Officer)
  • Richard A. Lewis (Issuing Officer)
View Company Profile

ID · 23a95032-ad8d-477f-b24d-0a5126ab27cc

Inspection Facts

Inspection number
1076420
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Abbott GmbH

5
DateClassificationOfficeProject area
May 23, 2025Not classifiedOffice of Inspections and Investigations
January 17, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 13, 2013NAICenter for Devices and Radiological HealthBioresearch Monitoring
February 9, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
September 23, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Abbott GmbH
  • FDA Inspection 1275591 - 2025-05-23
  • FDA Inspection 1202396 - 2023-01-17
  • FDA Inspection 839385 - 2013-06-13
  • FDA Inspection 770439 - 2012-02-09
  • FDA Inspection 684828 - 2010-09-23

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