FDA Inspection 1073462 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1032500

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

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.