# FDA Inspection 1102364 - Dolor Technologies LLC - September 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/dolor-technologies-llc/902298f6-6daa-4087-a737-f33367c2fb5d
Source feed: FDA_Inspections

> FDA Inspection 1102364 for Dolor Technologies LLC on September 19, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102364
- Company Name: Dolor Technologies LLC
- Inspection Date: 2019-09-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102364 - 2019-09-19](https://www.keypedia.com/records/fda_inspections/dolor-technologies-llc/63063c05-1423-4fe3-8e5c-6683d1563ef2)
- [FDA Inspection 1008362 - 2017-04-17](https://www.keypedia.com/records/fda_inspections/dolor-technologies-llc/e4ba135c-823c-41be-8965-c46634de4480)

Company: https://www.keypedia.com/companies/dolor-technologies-llc/dab077b4-fd5a-455c-a1b3-1b1ed500d75f

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