# FDA Inspection 1095737 - Titronics Research & Development Co. - July 09, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/titronics-research-development-co/0f6c343a-9e77-4f81-be34-05ccb5e2a8db
Source feed: FDA_Inspections

> FDA Inspection 1095737 for Titronics Research & Development Co. on July 09, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095737
- Company Name: Titronics Research & Development Co.
- Inspection Date: 2019-07-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1095737 - 2019-07-09](https://www.globalkeysolutions.net/records/fda_inspections/titronics-research-development-co/9595756a-b289-4b86-9994-e6a2d7e5e7d1)
- [FDA Inspection 876245 - 2014-04-16](https://www.globalkeysolutions.net/records/fda_inspections/titronics-research-development-co/cfc3fc77-eac4-4b13-9f3f-728808cc6d2f)
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Company: https://www.globalkeysolutions.net/companies/titronics-research-development-co/cb427513-a4b3-446a-8433-8053761a4f21

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