inforMED
FEI 3006648320

Philips North America Llc

222 Jacobs Street, Cambridge, MA, US

MDR events21,177All time
Recalls406All time
Registered products5
Establishment typeManufactureManufacture Medical Device

Registered product codes

5 product codes

Recalls

406 on file

Compliance history

Matched by FEI 3006648320.

FDA inspections

2 on file

  • Voluntary Action Indicated (VAI)Dec 13, 2023

    Compliance: Devices · Citations posted

  • No Action Indicated (NAI)Dec 13, 2023

    Postmarket Assurance: Devices · Citations posted

Inspection citations

3 on file

  • 21 CFR 820.90(a)Dec 13, 2023

    Nonconforming product, Lack of or inadequate procedures

  • 21 CFR 820.100(a)Dec 13, 2023

    Lack of or inadequate procedures

  • 21 CFR 820.198(a)Dec 13, 2023

    Lack of or inadequate complaint procedures

Compliance actions

0 on file

No warning letters or injunctions on file for this FEI number.