FDA Inspection 1331708 — Atalys Asheboro LLC

Atalys Asheboro LLC — FEI 1000111291

The FDA completed an inspection of Atalys Asheboro LLC on Aug 6, 2026 in Asheboro, NC. 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, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Asheboro, NC (United States)

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