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FDA Inspection
•Bausch & Lomb Incorporated•August 25, 2023

Bausch & Lomb Incorporated – FDA Inspection, Aug 25, 2023

Record Details

This FDA Inspection record concerns Bausch & Lomb Incorporated, with an inspection on August 25, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Bausch & Lomb Incorporated
Inspection Date
August 25, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Gretchen M. Laws (Issuing Officer)
  • Joanne E. King (FDA Associated Person)
  • Mabany Lizardi (Issuing Officer)
View Company Profile

ID · b911fb20-0187-4ef8-81b2-29e502aa8a51

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1218198
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Bausch & Lomb Incorporated

10
DateClassificationOfficeProject area
March 20, 2026Not classifiedFlorida District Office
January 30, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 10, 2018OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 26, 2017VAICenter for Drug Evaluation and ResearchNew Drug Evaluation
February 25, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 10 other inspections on the company page
Other documents for Bausch & Lomb Incorporated
  • FDA Inspection 1304548 - 2026-03-20
  • FDA Inspection 1082137 - 2019-01-30
  • FDA Inspection 1061913 - 2018-08-10
  • FDA Inspection 1015001 - 2017-05-26
  • FDA Inspection 967714 - 2016-02-25

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