FDA Inspection
Genoray Co LtdGenoray Co Ltd – FDA Inspection, Mar 21, 2013
Record Details
This FDA Inspection record concerns Genoray Co Ltd, with an inspection on March 21, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Genoray Co Ltd
- Inspection Date
- March 21, 2013
- Product Type
- Devices
View Company Profile
ID · 5ca4b348-fa2a-4342-a7b7-8493f373d22f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 824330
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 820.22Quality Audits - defined intervals
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Genoray Co Ltd
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 31, 2011 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Genoray Co Ltd
- FDA Inspection 733281 - 2011-05-31
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.