FDA Inspection
Zhejiang Clairvoyant Pharmaceutical Technology Co., Ltd.Zhejiang Clairvoyant Pharmaceutical Technology Co., Ltd. – FDA Inspection, Oct 27, 2023
Record Details
This FDA Inspection record concerns Zhejiang Clairvoyant Pharmaceutical Technology Co., Ltd., with an inspection on October 27, 2023, issued by the Office of Inspections and Investigations.
- Inspection Date
- October 27, 2023
View Company Profile
ID · 12478349-d0c1-4869-a5e6-b1a6138db772
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1223660
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.63Equipment Design, Size and Location
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Zhejiang Clairvoyant Pharmaceutical Technology Co., Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 16, 2025 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Clairvoyant Pharmaceutical Technology Co., Ltd.
- FDA Inspection 1280299 - 2025-07-16
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.