# Shenzhen Biocare Bio-Medical Equipment Co., Ltd. – FDA Inspection, Jan 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-biocare-bio-medical-equipment-co-ltd/00954df0-95bd-455e-8f5b-b9befc5e4c12
Source feed: FDA_Inspections

> FDA inspection 1080540 of Shenzhen Biocare Bio-Medical Equipment Co., Ltd., January 24, 2019. 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: 1080540
- Company Name: Shenzhen Biocare Bio-Medical Equipment Co., Ltd.
- Inspection Date: 2019-01-24
- 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 1258985 - 2024-11-22](https://www.keypedia.com/records/fda_inspections/shenzhen-biocare-bio-medical-equipment-co-ltd/3a512891-5824-4775-9326-432f37036125)

## Related Officers

- [Monica C. Burgos Garcia](https://www.keypedia.com/people/monica-c-burgos-garcia/d73d6ad6-4158-4c12-a0bf-6f5721db3400)

Company: https://www.keypedia.com/companies/shenzhen-biocare-bio-medical-equipment-co-ltd/d68cf9cc-0d10-4c31-9497-830867831184

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