# FDA Inspection 1284350 - Syntech International, Inc - September 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/syntech-international-inc/a0de050b-4370-4db4-9e02-d044a5ce0451
Source feed: FDA_Inspections

> FDA Inspection 1284350 for Syntech International, Inc on September 19, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1284350
- Company Name: Syntech International, Inc
- Inspection Date: 2025-09-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1284350 - 2025-09-19](https://www.keypedia.com/records/fda_inspections/syntech-international-inc/b25c5d68-9159-474b-be66-094a71f30691)
- [FDA Inspection 1284350 - 2025-09-19](https://www.keypedia.com/records/fda_inspections/syntech-international-inc/9233287a-faea-4440-97c6-c1295a02a7dc)
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Company: https://www.keypedia.com/companies/syntech-international-inc/f83b30aa-4538-43dd-834e-ef92c43329ca

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