FDA Inspection
Zhejiang Meimi Technology Co., Ltd.Zhejiang Meimi Technology Co., Ltd. – FDA Inspection, May 17, 2024
Record Details
This FDA Inspection record concerns Zhejiang Meimi Technology Co., Ltd., with an inspection on May 17, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · f48b9b6f-34ce-4281-8348-c9804a6bf01a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1241413
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
9- 21 CFR 211.68(b)Computer control of master formula records
- 21 CFR 211.196Distribution Record Requirements
- 21 CFR 211.46(b)Equipment for Environmental Control
- 21 CFR 211.63Equipment Design, Size and Location
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.194(a)(4)Complete Test Data
- 21 CFR 211.84(d)(1)Identity Testing of Each Component
- 21 CFR 211.22(c)Approve or reject procedures or specs
- 21 CFR 211.100(a)Absence of Written Procedures
Full citation text and observation details available on the Dashboard.
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.