# FDA Inspection 989483 - Syntech Development And Manufacturing Inc - September 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/syntech-development-and-manufacturing-inc/bc62b5c0-9d94-4ae1-8a02-cef51121fe8a
Source feed: FDA_Inspections

> FDA Inspection 989483 for Syntech Development And Manufacturing Inc on September 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989483
- Company Name: Syntech Development And Manufacturing Inc
- Inspection Date: 2016-09-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 739506 - 2011-07-27](https://www.keypedia.com/records/fda_inspections/syntech-development-and-manufacturing-inc/01e30d66-8308-487f-8951-06dcb86473c6)

Company: https://www.keypedia.com/companies/syntech-development-and-manufacturing-inc/9ea53120-620c-416c-b5a1-51e145f579a6

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