# FDA Inspection 588900 - Syntec Inc - June 12, 2009

Source: https://www.keypedia.com/records/fda_inspections/syntec-inc/c51ed9ee-b36e-468a-89ad-b7ac03f93cee
Source feed: FDA_Inspections

> FDA Inspection 588900 for Syntec Inc on June 12, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 588900
- Company Name: Syntec Inc
- Inspection Date: 2009-06-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/syntec-inc/962e37f5-0f96-4d4a-9647-662c13f4a86c

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