FDA inspection

Bausch & Lomb Incorporated: FDA inspection ending Jan 19, 2001

FDA inspection 59304 · No Action Indicated (NAI) · Wilmington, MA

Key facts

Inspection ID 59304
Firm Bausch & Lomb Incorporated
FEI number 1281950
Address 100 Research Dr
City Wilmington
State MA
ZIP 01887-4441
Fiscal year 2001
Inspection end date Jan 19, 2001
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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

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