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FDA Inspection 1042701 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1317628

The FDA completed an inspection of Bausch & Lomb Incorporated on February 23, 2018 in Rochester, NY. 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
February 23, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rochester, NY (United States)

Facility

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FDA data resources