FDA inspection

Lonza Biologics, Inc.: FDA inspection ending Feb 7, 2018

FDA inspection 1040839 · No Action Indicated (NAI) · Portsmouth, NH

Key facts

Inspection ID 1040839
Firm Lonza Biologics, Inc.
FEI number 3001451441
Address 101 International Dr
City Portsmouth
State NH
ZIP 03801-2846
Fiscal year 2018
Inspection end date Feb 7, 2018
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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