FDA Inspection
Cataki International Inc.Cataki International Inc. – FDA Inspection, Jul 11, 2013
Record Details
This FDA Inspection record concerns Cataki International Inc., with an inspection on July 11, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cataki International Inc.
- Inspection Date
- July 11, 2013
- Product Type
- Devices
View Company Profile
ID · fbf3dc05-0cc4-41d2-93b0-64ec5f06b7e2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 839886
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Cataki International Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 31, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Cataki International Inc.
- FDA Inspection 718477 - 2011-03-31
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.