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FDA Inspection
•Chengdu Shengnuo Biopharm Co Ltd•August 27, 2026

Chengdu Shengnuo Biopharm Co Ltd – FDA Inspection, Aug 27, 2026

Record Details

This FDA Inspection record concerns Chengdu Shengnuo Biopharm Co Ltd, with an inspection on August 27, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Chengdu Shengnuo Biopharm Co Ltd
Inspection Date
August 27, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Crystal Monroy
  • Marcellinus D. Dordunoo (FDA Associated Person)
  • Yoonhee Kim (Issuing Officer)
  • Youkeun Kim
View Company Profile

ID · 8579538b-d6b3-4b81-b520-51c8447f010d

Inspection Facts

Inspection number
1334998
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Chengdu Shengnuo Biopharm Co Ltd

4
DateClassificationOfficeProject area
September 8, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 10, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 9, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 24, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Chengdu Shengnuo Biopharm Co Ltd
  • FDA Inspection 1219460 - 2023-09-08
  • FDA Inspection 978495 - 2016-06-10
  • FDA Inspection 924616 - 2015-04-09
  • FDA Inspection 784098 - 2012-05-24

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