FDA inspection

Lonza Bend Inc.: FDA inspection ending Aug 5, 2022

FDA inspection 1176638 · Voluntary Action Indicated (VAI) · Bend, OR

Key facts

Inspection ID 1176638
Firm Lonza Bend Inc.
FEI number 1000656789
Address 64550 Research Rd
City Bend
State OR
ZIP 97703
Country United States
Fiscal year 2022
Inspection end date Aug 5, 2022
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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