# FDA Inspection 1266113 - Leltek Inc. - March 06, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/leltek-inc/964104f5-690d-4b30-af28-7ac3dfaa818a/
Source feed: FDA_Inspections

> FDA Inspection 1266113 for Leltek Inc. on March 06, 2025. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1266113
- Company Name: Leltek Inc.
- Inspection Date: 2025-03-06
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1266113 - 2025-03-06](https://www.globalkeysolutions.net/api/records/fda_inspections/leltek-inc/dfee7b16-d3a5-4da5-b763-0335a83e9bc8/)
- [FDA Inspection 1266113 - 2025-03-06](https://www.globalkeysolutions.net/api/records/fda_inspections/leltek-inc/ae5562ba-a617-4354-a58b-6d6ca7236fa0/)

Company: https://www.globalkeysolutions.net/companies/leltek-inc/72511bac-313b-4774-adbf-d12ddf42cd96

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