# Dolor Technologies LLC – FDA Inspection, Sep 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 of Dolor Technologies LLC, September 19, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1008362 - 2017-04-17](https://www.keypedia.com/records/fda_inspections/dolor-technologies-llc/e4ba135c-823c-41be-8965-c46634de4480)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

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