FDA Inspection
Holymed Products Co., Ltd.Holymed Products Co., Ltd. – FDA Inspection, Jun 19, 2019
Record Details
This FDA Inspection record concerns Holymed Products Co., Ltd., with an inspection on June 19, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Shaquenta Y. Perkins (Issuing Officer)
View Company Profile
ID · 9aba731a-1f1d-443d-9574-888e86ab5f41
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1095276
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Holymed Products Co., Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 13, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Holymed Products Co., Ltd.
- FDA Inspection 926644 - 2015-05-13
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.