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FDA Inspection
•Planet (Suzhou) Medical Products Co., Ltd.•September 27, 2017

Planet (Suzhou) Medical Products Co., Ltd. – FDA Inspection, Sep 27, 2017

Record Details

This FDA Inspection record concerns Planet (Suzhou) Medical Products Co., Ltd., with an inspection on September 27, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Planet (Suzhou) Medical Products Co., Ltd.
Inspection Date
September 27, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Sandra A. Boyd (Investigator)
View Company Profile

ID · 946ebbc0-f0ef-48fd-a319-9d91b714d1c2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1029000
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Planet (Suzhou) Medical Products Co., Ltd.

2
DateClassificationOfficeProject area
August 31, 2017Not classifiedOffice of Inspections and Investigations
July 3, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Planet (Suzhou) Medical Products Co., Ltd.
  • FDA Inspection 1025334 - 2017-08-31
  • FDA Inspection 900565 - 2014-07-03

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