FDA Inspection 695485 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1000113778

The FDA completed an inspection of Bausch & Lomb Incorporated on Oct 25, 2010 in Tampa, FL. 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
Oct 25, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Tampa, FL (United States)

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