# FDA Inspection 1276305 - L Z FORM KFT - June 18, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/l-z-form-kft/f00c52ef-a72e-4af9-952f-263940b71ad1
Source feed: FDA_Inspections

> FDA Inspection 1276305 for L Z FORM KFT on June 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276305
- Company Name: L Z FORM KFT
- Inspection Date: 2025-06-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276305 - 2025-06-18](https://www.globalkeysolutions.net/records/fda_inspections/l-z-form-kft/5b799468-4505-4e39-8413-8d85a961be6f)
- [FDA Inspection 1276305 - 2025-06-18](https://www.globalkeysolutions.net/records/fda_inspections/l-z-form-kft/df658e19-81c1-4c8a-bad9-4d7ca49320d2)
- [FDA Inspection 1276305 - 2025-06-18](https://www.globalkeysolutions.net/records/fda_inspections/l-z-form-kft/0cb18b4a-5e09-4356-b4fa-728f69bdf780)

Company: https://www.globalkeysolutions.net/companies/l-z-form-kft/5d57052d-2e74-4764-9cda-dabc131ec2bc

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7