# Guangzhou Improve Medical Instruments Co., Ltd. – FDA Inspection, Nov 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/guangzhou-improve-medical-instruments-co-ltd/ea17f5cf-58e4-49c3-aaa7-06001dc7332d
Source feed: FDA_Inspections

> FDA inspection 1038626 of Guangzhou Improve Medical Instruments Co., Ltd., November 30, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038626
- Company Name: Guangzhou Improve Medical Instruments Co., Ltd.
- Inspection Date: 2017-11-30
- 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 912507 - 2015-01-17](https://www.keypedia.com/records/fda_inspections/guangzhou-improve-medical-instruments-co-ltd/da48c58f-0eb5-4ea9-b09f-f9efcfa06863)

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

Company: https://www.keypedia.com/companies/guangzhou-improve-medical-instruments-co-ltd/946ac81f-e9b4-4324-88cb-515519bd9221

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