# FDA Inspection 1019338 - CivaTech Oncology Inc. - May 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/civatech-oncology-inc/d4515a83-ba32-4002-b38b-9b986e9316ea
Source feed: FDA_Inspections

> FDA Inspection 1019338 for CivaTech Oncology Inc. on May 24, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1019338
- Company Name: CivaTech Oncology Inc.
- Inspection Date: 2017-05-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1208025 - 2023-06-14](https://www.keypedia.com/records/fda_inspections/civatech-oncology-inc/aed0dd62-7864-4c5c-8de7-a7ea48755c1a)
- [FDA Inspection 1208025 - 2023-06-14](https://www.keypedia.com/records/fda_inspections/civatech-oncology-inc/e75e6a6e-38ff-49a1-905a-56bc8af12941)
- [FDA Inspection 1019338 - 2017-05-24](https://www.keypedia.com/records/fda_inspections/civatech-oncology-inc/3e937bc8-96ee-4ad1-af13-7f858b6f4600)

Company: https://www.keypedia.com/companies/civatech-oncology-inc/1a0f5137-154e-43c6-b7ff-3b0a2d799001

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