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FDA Inspection
•Bausch & Lomb Incorporated•August 9, 2018

Bausch & Lomb Incorporated – FDA Inspection, Aug 9, 2018

Record Details

This FDA Inspection record concerns Bausch & Lomb Incorporated, with an inspection on August 9, 2018, issued by the New England District Office, covering medical devices & rad health.

Company
Bausch & Lomb Incorporated
Inspection Date
August 9, 2018
Product Type
Medical Devices & Rad Health
Office
New England District Office
View Company Profile

ID · 4aa7ea27-0bb7-405d-b8be-70c92b0a5d05

Inspection Facts

Inspection number
1157054
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Bausch & Lomb Incorporated

2
DateClassificationOfficeProject area
July 31, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
April 18, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Bausch & Lomb Incorporated
  • FDA Inspection 843014 - 2013-07-31
  • FDA Inspection 720310 - 2011-04-18

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