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FDA Inspection
•Alcon Research LLC•August 20, 2013

Alcon Research LLC – FDA Inspection, Aug 20, 2013

Record Details

This FDA Inspection record concerns Alcon Research LLC, with an inspection on August 20, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Alcon Research LLC
Inspection Date
August 20, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 3ae2edfa-a4c2-46ff-be25-881ec4bd8678

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
847586
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

FDA Citations

1
  1. 21 CFR 812.140(b)(2)Sponsor device disposition records inadequate

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Alcon Research LLC

18
DateClassificationOfficeProject area
June 22, 2026Not classifiedDallas District Office
August 30, 2024Not classifiedDallas District OfficeDrug Quality Assurance
September 15, 2022NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
October 24, 2019NAICenter for Devices and Radiological HealthBioresearch Monitoring
September 24, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 18 other inspections on the company page
Other documents for Alcon Research LLC
  • FDA Inspection 1313496 - 2026-06-22
  • FDA Inspection 1230060 - 2024-08-30
  • FDA Inspection 1180688 - 2022-09-15
  • FDA Inspection 1112448 - 2019-10-24
  • FDA Inspection 1070484 - 2018-09-24

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