FDA Inspection 1177825 — Marox Corporation

Marox Corporation — FEI 1219213

The FDA completed an inspection of Marox Corporation on July 22, 2022 in Holyoke, 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
July 22, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Holyoke, MA (United States)