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FDA Inspection 1031429 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1032500

The FDA completed an inspection of Bausch & Lomb Incorporated on September 15, 2017 in Greenville, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 15, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greenville, SC (United States)

Facility

Other inspections at this facility

  • 1250877 (OAI Thu Feb 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1073462 (NAI Tue Aug 28 2018 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