# Anhui Kangda Medical Products Co., Ltd. – FDA Inspection, Jun 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/anhui-kangda-medical-products-co-ltd/c1059927-328a-4dd3-962d-f0d54daa56a1
Source feed: FDA_Inspections

> FDA inspection 1056979 of Anhui Kangda Medical Products Co., Ltd., June 13, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056979
- Company Name: Anhui Kangda Medical Products Co., Ltd.
- Inspection Date: 2018-06-13
- 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: 0

## Related Documents

- [FDA Inspection 907776 - 2014-11-20](https://www.keypedia.com/records/fda_inspections/anhui-kangda-medical-products-co-ltd/9fa8278f-d774-4fb6-a05a-65716109f262)
- FDA Inspection 907781 - 2014-11-19

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-z-lu/17448aca-e316-424c-b7b2-88c8baffc359)

Company: https://www.keypedia.com/companies/anhui-kangda-medical-products-co-ltd/9da017f1-ba1a-4682-a080-835c54bbcff4

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