FDA Inspection 1276305 — L Z FORM KFT

L Z FORM KFT — FEI 3008215723

The FDA completed an inspection of L Z FORM KFT on Jun 18, 2025 in Ajka. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 18, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ajka (Hungary)

Citations

IDCFRDescription
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.