# FDA Inspection 1182153 - Philips North America LLC - October 27, 2022

Source: https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/c3c38841-45c1-4d4e-bacd-8cb043014c7c
Source feed: FDA_Inspections

> FDA Inspection 1182153 for Philips North America LLC on October 27, 2022. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1182153
- Company Name: Philips North America LLC
- Inspection Date: 2022-10-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1292226 - 2025-11-21](https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/e2bae125-8c4a-4f6a-9532-aef671cb6fd0)
- [FDA Inspection 1292226 - 2025-11-21](https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/b25dfe5c-f2be-4b09-859f-625f96410493)
- [FDA Inspection 1236344 - 2024-11-06](https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/1176b39b-a609-4759-98c0-c2bbb07d6235)
- [FDA Inspection 1236344 - 2024-11-06](https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/7ffed61f-639b-4689-bac4-799001fc4a1a)
- [FDA Inspection 1182153 - 2022-10-27](https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/45d5375b-4a70-477c-872a-3af00d9aa35e)

Company: https://www.keypedia.com/companies/philips-north-america-llc/d7335702-bc34-4fb8-acdc-db91e81d2f8c

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