FDA inspection

Bausch & Lomb Incorporated: FDA inspection ending Aug 9, 2018

FDA inspection 1157054 · Voluntary Action Indicated (VAI) · Wilmington, MA

Key facts

Inspection ID 1157054
Firm Bausch & Lomb Incorporated
FEI number 1281950
Address 100 Research Dr
City Wilmington
State MA
ZIP 01887-4441
Fiscal year 2018
Inspection end date Aug 9, 2018
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

Browse all FDA inspections