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FDA Inspection
•Bausch & Lomb Ireland Limited•July 1, 2022

Bausch & Lomb Ireland Limited – FDA Inspection, Jul 1, 2022

Record Details

This FDA Inspection record concerns Bausch & Lomb Ireland Limited, with an inspection on July 1, 2022, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Bausch & Lomb Ireland Limited
Inspection Date
July 1, 2022
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · dcc4b56d-b01d-40b0-8bef-983a799545ec

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1179049
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Bausch & Lomb Ireland Limited

5
DateClassificationOfficeProject area
November 16, 2018Not classifiedOffice of Inspections and Investigations
September 15, 2017Not classifiedOffice of Inspections and Investigations
February 17, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 9, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
July 21, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Bausch & Lomb Ireland Limited
  • FDA Inspection 1102223 - 2018-11-16
  • FDA Inspection 1042514 - 2017-09-15
  • FDA Inspection 1008319 - 2017-02-17
  • FDA Inspection 744844 - 2011-08-09
  • FDA Inspection 739708 - 2011-07-21

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