# Transonic Systems Inc – FDA Inspection, Jun 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/transonic-systems-inc/8fe72704-6e24-4fd7-8f03-b18ec0298776
Source feed: FDA_Inspections

> FDA inspection 1015982 of Transonic Systems Inc, June 16, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015982
- Company Name: Transonic Systems Inc
- Inspection Date: 2017-06-16
- 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: 5

## Related Documents

- [FDA Inspection 1040245 - 2018-02-01](https://www.keypedia.com/records/fda_inspections/transonic-systems-inc/b0f41e84-e83c-4c92-94ec-b36db1c00a7d)
- FDA Inspection 860000 - 2013-11-19
- [FDA Inspection 823936 - 2013-03-21](https://www.keypedia.com/records/fda_inspections/transonic-systems-inc/f87181a8-e810-41f3-a846-d0c3b42dc9d9)
- FDA Inspection 643524 - 2010-01-26

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-c-mendiola/387f053a-af5f-4da9-8042-031124b9467d)

Company: https://www.keypedia.com/companies/transonic-systems-inc/e7fccd95-e2f9-4c0d-abbf-0afd4829e33d

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