# FDA Inspection 1094170 - Xtreem Pulse LLC - June 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/xtreem-pulse-llc/9a94f8c4-e6da-4195-a4a6-3481209564f0
Source feed: FDA_Inspections

> FDA Inspection 1094170 for Xtreem Pulse LLC on June 19, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1094170
- Company Name: Xtreem Pulse LLC
- Inspection Date: 2019-06-19
- 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 1220381 - 2023-10-13](https://www.keypedia.com/records/fda_inspections/xtreem-pulse-llc/7ad0af4d-2796-4a3e-9224-57860f7ed8aa)
- [FDA Inspection 1220381 - 2023-10-13](https://www.keypedia.com/records/fda_inspections/xtreem-pulse-llc/cf8852fb-41d1-4a36-8147-63331520de52)
- [FDA Inspection 1173093 - 2022-06-29](https://www.keypedia.com/records/fda_inspections/xtreem-pulse-llc/05c81fe9-fe82-4b6f-b882-a2200062a446)
- [FDA Inspection 1173093 - 2022-06-29](https://www.keypedia.com/records/fda_inspections/xtreem-pulse-llc/40d62047-b27b-4d30-9343-6de93b56694d)
- [FDA Inspection 1094170 - 2019-06-19](https://www.keypedia.com/records/fda_inspections/xtreem-pulse-llc/019dce03-f1fb-4dda-ad78-a8a1bf23be61)

Company: https://www.keypedia.com/companies/xtreem-pulse-llc/4369da2f-f49e-455a-97cd-8b3efa71f387

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