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FDA Inspection 950005 — Bausch & Lomb Surgical, Inc.

Bausch & Lomb Surgical, Inc. — FEI 1119279

The FDA completed an inspection of Bausch & Lomb Surgical, Inc. on November 30, 2015 in Clearwater, FL. 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
November 30, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Clearwater, FL (United States)

Facility

Other inspections at this facility

  • 1030850 (VAI Fri Nov 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1008783 (VAI Wed Apr 05 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 926666 (VAI Mon May 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841984 (VAI Mon Jul 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 749104 (NAI Fri Oct 07 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources