FDA Inspection
Kinamed IncKinamed Inc – FDA Inspection, Aug 27, 2026
Record Details
This FDA Inspection record concerns Kinamed Inc, with an inspection on August 27, 2026, issued by the Los Angeles District Office, covering medical devices & rad health.
View Company Profile
ID · dccd1e54-3824-4675-bd89-fe671aeeb8d2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1333118
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- ISO 13485:2016 Clause 8.2.6Monitoring and measurement requirements of product characteristics are not met
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Kinamed Inc
6| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 21, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 14, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 15, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 1, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kinamed Inc
- FDA Inspection 1117751 - 2020-02-12
- FDA Inspection 980471 - 2016-07-21
- FDA Inspection 875744 - 2014-04-14
- FDA Inspection 773213 - 2012-03-15
- FDA Inspection 663654 - 2010-06-01
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.