FDA Inspection 1123430 — DYSIS Medical Inc

DYSIS Medical Inc — FEI 3010628103

The FDA completed an inspection of DYSIS Medical Inc on March 9, 2020 in Natick, 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
March 9, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Natick, MA (United States)