FDA Inspection 1228351 — THE LINDEN GROUP CORP.

THE LINDEN GROUP CORP. — FEI 3012336461

The FDA completed an inspection of THE LINDEN GROUP CORP. on Dec 13, 2023 in Cedar Knolls, NJ. 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
Dec 13, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Cedar Knolls, NJ (United States)