# Sanara Pulsar, LLC – FDA Inspection, Aug 6, 2019

Source: https://www.keypedia.com/records/fda_inspections/sanara-pulsar-llc/d716df9b-62cf-43ba-be66-b3524a22a3fc
Source feed: FDA_Inspections

> FDA inspection 1101597 of Sanara Pulsar, LLC, August 06, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101597
- Company Name: Sanara Pulsar, LLC
- Inspection Date: 2019-08-06
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/marcia-g-evans/2e20a31d-0267-4040-b1a1-c0bec23b964b)
- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)
- [Issuing Officer](https://www.keypedia.com/people/tuan-a-nguyen/50723bbb-29a1-4e7a-a5aa-123ec3866065)

Company: https://www.keypedia.com/companies/sanara-pulsar-llc/d2a32017-7281-4699-bd2d-415864d94c20

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