# FDA Inspection 1260630 - Philips DS North America LLC - January 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/philips-ds-north-america-llc/a4ef9e10-b164-4e05-92cb-7b1d344cc6aa
Source feed: FDA_Inspections

> FDA Inspection 1260630 for Philips DS North America LLC on January 16, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260630
- Company Name: Philips DS North America LLC
- Inspection Date: 2025-01-16
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices

## Related Documents

- [FDA Inspection 1260630 - 2025-01-16](https://www.keypedia.com/records/fda_inspections/philips-ds-north-america-llc/efe04086-0bb7-4f05-a448-0dfc6ef7fb42)

Company: https://www.keypedia.com/companies/philips-ds-north-america-llc/1670f782-b662-4827-8dbb-15bc7de82ad2