FDA Inspection 1100134 — Acuity Surgical Devices, LLC

Acuity Surgical Devices, LLC — FEI 3010866843

The FDA completed an inspection of Acuity Surgical Devices, LLC on Aug 1, 2019 in Irving, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 1, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Irving, TX (United States)

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