FDA Inspection 1101597 — Sanara Pulsar, LLC

Sanara Pulsar, LLC — FEI 3013383038

The FDA completed an inspection of Sanara Pulsar, LLC on Aug 6, 2019 in Fort Worth, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 6, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fort Worth, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.