# FDA Inspection 1269239 - Earlitec Diagnostics - May 01, 2025

Source: https://www.keypedia.com/records/fda_inspections/earlitec-diagnostics/e3318ba4-9077-432a-924c-47584ceeba1c
Source feed: FDA_Inspections

> FDA Inspection 1269239 for Earlitec Diagnostics on May 01, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1269239
- Company Name: Earlitec Diagnostics
- Inspection Date: 2025-05-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1269239 - 2025-05-01](https://www.keypedia.com/records/fda_inspections/earlitec-diagnostics/b70e2436-f81e-4690-8ff7-cf2127d75890)

Company: https://www.keypedia.com/companies/earlitec-diagnostics/83a51881-c0cf-4747-965f-87eecc64d9d3

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