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FDA Inspection
•Jumin Bio-Technologies Co., Ltd•May 16, 2019

Jumin Bio-Technologies Co., Ltd – FDA Inspection, May 16, 2019

Record Details

This FDA Inspection record concerns Jumin Bio-Technologies Co., Ltd, with an inspection on May 16, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Jumin Bio-Technologies Co., Ltd
Inspection Date
May 16, 2019
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Jacqueline S. Warner (Issuing Officer)
View Company Profile

ID · db3ad627-79c8-44a8-9836-559060425553

Inspection Facts

Inspection number
1093981
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
  2. 21 CFR 820.75(c)Documentation - review in response to changes or deviations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Jumin Bio-Technologies Co., Ltd

3
DateClassificationOfficeProject area
May 25, 2024VAICenter for Devices and Radiological HealthCompliance: Devices
May 29, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
January 28, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Jumin Bio-Technologies Co., Ltd
  • FDA Inspection 1243902 - 2024-05-25
  • FDA Inspection 885560 - 2014-05-29
  • FDA Inspection 709725 - 2011-01-28

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