# FDA Inspection 1008362 - Dolor Technologies LLC - April 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/dolor-technologies-llc/e4ba135c-823c-41be-8965-c46634de4480
Source feed: FDA_Inspections

> FDA Inspection 1008362 for Dolor Technologies LLC on April 17, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008362
- Company Name: Dolor Technologies LLC
- Inspection Date: 2017-04-17
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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