FDA Inspection
Beijing Aeonmed Company LimitedBeijing Aeonmed Company Limited – FDA Inspection, Jul 18, 2019
Record Details
This FDA Inspection record concerns Beijing Aeonmed Company Limited, with an inspection on July 18, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Teresa K. Kastner
View Company Profile
ID · a6d818fd-ef54-4af2-b0c3-c2e687d5c595
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1099707
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.80(e)Documentation
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.