# FDA Inspection 834864 - Kanteron Systems USA, Inc. - May 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/kanteron-systems-usa-inc/b5191768-9407-4e3e-adf8-c3d6d5dfb319
Source feed: FDA_Inspections

> FDA Inspection 834864 for Kanteron Systems USA, Inc. on May 13, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 834864
- Company Name: Kanteron Systems USA, Inc.
- Inspection Date: 2013-05-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 912971 - 2015-02-05](https://www.keypedia.com/records/fda_inspections/kanteron-systems-usa-inc/bef21bbe-f4fa-4725-8019-ca1a662e84f1)
- [FDA Inspection 834864 - 2013-05-13](https://www.keypedia.com/records/fda_inspections/kanteron-systems-usa-inc/2b084dfd-525f-42f1-a9fe-d300f6af6104)

Company: https://www.keypedia.com/companies/kanteron-systems-usa-inc/a7413066-5986-453b-9c61-97993d1bbcb7

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7