# FDA Inspection 1004504 - Florida Probe Corporation - February 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/florida-probe-corporation/7d7b29fe-97e3-4d71-b829-1fd8b118d947
Source feed: FDA_Inspections

> FDA Inspection 1004504 for Florida Probe Corporation on February 14, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004504
- Company Name: Florida Probe Corporation
- Inspection Date: 2017-02-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1004504 - 2017-02-14](https://www.keypedia.com/records/fda_inspections/florida-probe-corporation/b58b6c2c-5f98-4090-8db4-8562fd4ae66a)
- [FDA Inspection 893114 - 2014-08-28](https://www.keypedia.com/records/fda_inspections/florida-probe-corporation/8d4c10a8-c2f0-4751-8ab2-627c69832ca3)
- [FDA Inspection 893114 - 2014-08-28](https://www.keypedia.com/records/fda_inspections/florida-probe-corporation/69c5618c-bd5c-40da-88bf-a456acf3fa2f)

Company: https://www.keypedia.com/companies/florida-probe-corporation/60258f16-c5d0-439f-b1ef-b90c41876d18

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