FDA inspection

LEVO AG: FDA inspection ending Apr 9, 2025

FDA inspection 1266290 · Official Action Indicated (OAI) · Wohlen Ag

Key facts

Inspection ID 1266290
Firm LEVO AG
FEI number 1000268398
Address Angliker Strasse 20
City Wohlen Ag
Country Switzerland
Fiscal year 2025
Inspection end date Apr 9, 2025
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 717287

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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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