FDA Inspection
JOOWON INNOVATION CO, LTDJOOWON INNOVATION CO, LTD – FDA Inspection, Jan 18, 2024
Record Details
This FDA Inspection record concerns JOOWON INNOVATION CO, LTD, with an inspection on January 18, 2024, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · e9ba64ec-3f03-465e-ac96-180bb7e139d9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1227185
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.198(a)Complaints
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
Full citation text and observation details available on the Dashboard.
Other FDA inspections of JOOWON INNOVATION CO, LTD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 17, 2026 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
Other documents for JOOWON INNOVATION CO, LTD
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.