FDA Inspection 1180446 — Gentuity, LLC

Gentuity, LLC — FEI 3011578544

The FDA completed an inspection of Gentuity, LLC on September 16, 2022 in Sudbury, MA. 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
September 16, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Sudbury, MA (United States)