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FDA Inspection
•Shenzhen Biocare Bio-Medical Equipment Co., Ltd.•January 24, 2019

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

Record Details

This FDA Inspection record concerns Shenzhen Biocare Bio-Medical Equipment Co., Ltd., with an inspection on January 24, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Shenzhen Biocare Bio-Medical Equipment Co., Ltd.
Inspection Date
January 24, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Monica C. Burgos Garcia
View Company Profile

ID · 00954df0-95bd-455e-8f5b-b9befc5e4c12

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1080540
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Shenzhen Biocare Bio-Medical Equipment Co., Ltd.

1
DateClassificationOfficeProject area
November 22, 2024OAICompliance: Devices
Other documents for Shenzhen Biocare Bio-Medical Equipment Co., Ltd.
  • FDA Inspection 1258985 - 2024-11-22

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