# FDA Inspection 1099964 - Wisdom Medical Technologies - August 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/wisdom-medical-technologies/2d78a3cd-6483-4564-91df-16218af8b61b
Source feed: FDA_Inspections

> FDA Inspection 1099964 for Wisdom Medical Technologies on August 19, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1099964
- Company Name: Wisdom Medical Technologies
- Inspection Date: 2019-08-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1099964 - 2019-08-19](https://www.keypedia.com/records/fda_inspections/wisdom-medical-technologies/32a567a7-7664-4784-a264-c6de76ff7278)
- [FDA Inspection 1099964 - 2019-08-19](https://www.keypedia.com/records/fda_inspections/wisdom-medical-technologies/8028304b-afa8-4865-87c8-74716b73564c)

Company: https://www.keypedia.com/companies/wisdom-medical-technologies/db794f76-a978-4b6a-8a7f-796c9f986d13

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