FDA Inspection
Suzhou Amerigen Pharmaceutical Co., Ltd.Suzhou Amerigen Pharmaceutical Co., Ltd. – FDA Inspection, Nov 11, 2016
Record Details
This FDA Inspection record concerns Suzhou Amerigen Pharmaceutical Co., Ltd., with an inspection on November 11, 2016, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- November 11, 2016
- Product Type
- Human Drugs
View Company Profile
ID · d137c4f6-ea68-4e76-8f21-7875963cbff9
Inspection Facts
- Inspection number
- 992992
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Suzhou Amerigen Pharmaceutical Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 25, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 19, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 19, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 3, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Suzhou Amerigen Pharmaceutical Co., Ltd.
- FDA Inspection 1030228 - 2017-10-25
- FDA Inspection 935610 - 2015-06-19
- FDA Inspection 852974 - 2013-07-19
- FDA Inspection 617851 - 2009-09-03
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