# FDA Inspection 1094122 - Syntech International, Inc - May 09, 2019

Source: https://www.keypedia.com/records/fda_inspections/syntech-international-inc/d26aff7b-e613-4ae3-a805-5a67c731b8b8
Source feed: FDA_Inspections

> FDA Inspection 1094122 for Syntech International, Inc on May 09, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094122
- Company Name: Syntech International, Inc
- Inspection Date: 2019-05-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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