FDA Inspection 1101597 — Sanara Pulsar, LLC
The FDA completed an inspection of Sanara Pulsar, LLC on August 6, 2019 in Fort Worth, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 6, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Fort Worth, TX (United States)