# FDA Inspection 883866 - Lincotek Medical - June 18, 2014

Source: https://www.keypedia.com/records/fda_inspections/lincotek-medical/b1351163-afc8-4878-a10a-dc679febd0d1
Source feed: FDA_Inspections

> FDA Inspection 883866 for Lincotek Medical on June 18, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 883866
- Company Name: Lincotek Medical
- Inspection Date: 2014-06-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1053006 - 2018-04-05](https://www.keypedia.com/records/fda_inspections/lincotek-medical/17eec8c6-d348-43dd-a3b9-1b579b634da2)
- [FDA Inspection 1053006 - 2018-04-05](https://www.keypedia.com/records/fda_inspections/lincotek-medical/b8c6ccff-6fa3-4ad0-b7aa-740c2e83e685)
- [FDA Inspection 883866 - 2014-06-18](https://www.keypedia.com/records/fda_inspections/lincotek-medical/09b0b170-1f08-4c15-8147-37cd446865cf)

Company: https://www.keypedia.com/companies/lincotek-medical/0ce4dc26-0bad-4f74-bcf8-ab97b29678af

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