FDA Inspection 1180446 — Gentuity, LLC

Gentuity, LLC — FEI 3011578544

The FDA completed an inspection of Gentuity, LLC on Sep 16, 2022 in Sudbury, MA. 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
Sep 16, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Sudbury, MA (United States)

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