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FDA Inspection 1073462 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1032500

The FDA completed an inspection of Bausch & Lomb Incorporated on August 28, 2018 in Greenville, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 28, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Greenville, SC (United States)

Facility

Other inspections at this facility

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  • 1031429 (NAI Fri Sep 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988726 (VAI Wed Oct 05 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 911396 (NAI Thu Jan 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 820858 (VAI Fri Feb 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources