# FDA Inspection 962509 - C-Axis PR., Inc. - February 19, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/c-axis-pr-inc/0c57f5c6-8f6d-486c-849f-5119bf3f6dcc
Source feed: FDA_Inspections

> FDA Inspection 962509 for C-Axis PR., Inc. on February 19, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 962509
- Company Name: C-Axis PR., Inc.
- Inspection Date: 2016-02-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1252463 - 2024-10-24](https://www.globalkeysolutions.net/records/fda_inspections/c-axis-pr-inc/422e87d2-4b1d-481f-bab5-b26a0d61a14b)
- [FDA Inspection 1252463 - 2024-10-24](https://www.globalkeysolutions.net/records/fda_inspections/c-axis-pr-inc/7986512e-647d-4ef3-b52a-2869331215d5)
- [FDA Inspection 1123270 - 2020-03-12](https://www.globalkeysolutions.net/records/fda_inspections/c-axis-pr-inc/2e426007-7a6b-4711-a176-532adce1da14)

Company: https://www.globalkeysolutions.net/companies/c-axis-pr-inc/506191b4-b878-442d-b0d7-44379c691b7a

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