# Headstar Medical Products Co., Ltd. – FDA Inspection, Dec 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/headstar-medical-products-co-ltd/1877d3b0-65ff-4155-8d3e-bcddfdbd7b1f
Source feed: FDA_Inspections

> FDA inspection 994816 of Headstar Medical Products Co., Ltd., December 15, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994816
- Company Name: Headstar Medical Products Co., Ltd.
- Inspection Date: 2016-12-15
- 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: 1

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- [FDA Inspection 636134 - 2009-11-05](https://www.keypedia.com/records/fda_inspections/headstar-medical-products-co-ltd/120bed40-271a-4d66-ac88-5dc88c778a9a)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/headstar-medical-products-co-ltd/c9e05d9e-3480-46b4-8a4b-40eb6b527e2b

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