FDA inspection

TYROMOTION GMBH: FDA inspection ending Jun 4, 2026

FDA inspection 1326082 · No Action Indicated (NAI) · Graz

Key facts

Inspection ID 1326082
Firm TYROMOTION GMBH
FEI number 3008887767
Address Bahnhofgurtel 59
City Graz
Country Austria
Fiscal year 2026
Inspection end date Jun 4, 2026
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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