# FDA Inspection 780786 - Philips Ultrasound( Shanghai) Co. Ltd. - April 05, 2012

Source: https://www.keypedia.com/records/fda_inspections/philips-ultrasound-shanghai-co-ltd/0249a2f6-c8e4-4ffb-97cf-55fca59354d0
Source feed: FDA_Inspections

> FDA Inspection 780786 for Philips Ultrasound( Shanghai) Co. Ltd. on April 05, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 780786
- Company Name: Philips Ultrasound( Shanghai) Co. Ltd.
- Inspection Date: 2012-04-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 780786 - 2012-04-05](https://www.keypedia.com/records/fda_inspections/philips-ultrasound-shanghai-co-ltd/a7c4c963-6c81-4396-8688-742cf42ea240)

Company: https://www.keypedia.com/companies/philips-ultrasound-shanghai-co-ltd/53f3d9a4-1955-4fc8-bc4b-1c6ab6a62fc5

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