# FDA Inspection 860000 - Transonic Systems Inc - November 19, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/transonic-systems-inc/08caadef-affd-4745-bd4b-c8c9cbd02918
Source feed: FDA_Inspections

> FDA Inspection 860000 for Transonic Systems Inc on November 19, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860000
- Company Name: Transonic Systems Inc
- Inspection Date: 2013-11-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1040245 - 2018-02-01](https://www.globalkeysolutions.net/records/fda_inspections/transonic-systems-inc/b0f41e84-e83c-4c92-94ec-b36db1c00a7d)
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- [FDA Inspection 860000 - 2013-11-19](https://www.globalkeysolutions.net/records/fda_inspections/transonic-systems-inc/18340376-58df-4ba2-a20f-82318b7272ed)

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

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