FDA inspection

Ricola Ag: FDA inspection ending Feb 18, 2022

FDA inspection 1163826 · Voluntary Action Indicated (VAI) · Laufen

Key facts

Inspection ID 1163826
Firm Ricola Ag
FEI number 1000170866
Address Baselstrasse 31
City Laufen
Country Switzerland
Fiscal year 2022
Inspection end date Feb 18, 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

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