# Philips Medical Systems Technologies Ltd – FDA Inspection, Jan 12, 2023

Source: https://www.keypedia.com/records/fda_inspections/philips-medical-systems-technologies-ltd/a38a3b0e-9f85-4ff8-8118-6cdb31387a12
Source feed: FDA_Inspections

> FDA inspection 1195326 of Philips Medical Systems Technologies Ltd, January 12, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195326
- Company Name: Philips Medical Systems Technologies Ltd
- Inspection Date: 2023-01-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1126550 - 2019-09-05

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

Company: https://www.keypedia.com/companies/philips-medical-systems-technologies-ltd/6352fe6a-1ccc-454f-94e3-bca45fd0334b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7