# FDA Inspection 739506 - Syntech Development And Manufacturing Inc - July 27, 2011

Source: https://www.keypedia.com/records/fda_inspections/syntech-development-and-manufacturing-inc/01e30d66-8308-487f-8951-06dcb86473c6
Source feed: FDA_Inspections

> FDA Inspection 739506 for Syntech Development And Manufacturing Inc on July 27, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 739506
- Company Name: Syntech Development And Manufacturing Inc
- Inspection Date: 2011-07-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 989483 - 2016-09-19](https://www.keypedia.com/records/fda_inspections/syntech-development-and-manufacturing-inc/bc62b5c0-9d94-4ae1-8a02-cef51121fe8a)

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