FDA Inspection
Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant)Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant) – FDA Inspection, Dec 15, 2017
Record Details
This FDA Inspection record concerns Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant), with an inspection on December 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- December 15, 2017
- Product Type
- Drugs
View Company Profile
ID · e45c89a3-ca11-49f0-80cb-5be00943133e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1037659
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant)
5| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2025 | Not classified | Office of Inspections and Investigations | |
| May 10, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 23, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 1, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 30, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant)
- FDA Inspection 1295032 - 2025-10-31
- FDA Inspection 1289802 - 2023-05-10
- FDA Inspection 1112213 - 2019-10-23
- FDA Inspection 892301 - 2014-08-01
- FDA Inspection 661070 - 2010-04-30
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