# Syntec Scientific Corporation – FDA Inspection, Dec 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/syntec-scientific-corporation/f8567c5a-c888-4693-ab36-8c7207e3de2f
Source feed: FDA_Inspections

> FDA inspection 1081598 of Syntec Scientific Corporation, December 13, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1081598
- Company Name: Syntec Scientific Corporation
- Inspection Date: 2018-12-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 908743 - 2014-12-18](https://www.keypedia.com/records/fda_inspections/syntec-scientific-corporation/db681d1f-d834-4f31-a01d-385ea2a8ea01)
- [FDA Inspection 671677 - 2010-07-01](https://www.keypedia.com/records/fda_inspections/syntec-scientific-corporation/f15156c1-0932-4d7b-a09d-3aa5c018a569)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gregson-a-joseph/90bf8118-3f32-4f44-95c4-fcde1f741a18)

Company: https://www.keypedia.com/companies/syntec-scientific-corporation/b9fced07-7baa-4f28-8df9-60fcb2ceea09

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