FDA inspection

L Z FORM KFT: FDA inspection ending Jun 18, 2025

FDA inspection 1276305 · Voluntary Action Indicated (VAI) · Ajka

Key facts

Inspection ID 1276305
Firm L Z FORM KFT
FEI number 3008215723
Address Ipari Park Nyugat Hrsz. 5704/4
City Ajka
Country Hungary
Fiscal year 2025
Inspection end date Jun 18, 2025
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

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