# FDA Inspection 1051621 - Lincotek Medical - April 02, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/lincotek-medical/fe39fb8d-25a5-46f5-867e-8bf3f21dc025/
Source feed: FDA_Inspections

> FDA Inspection 1051621 for Lincotek Medical on April 02, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051621
- Company Name: Lincotek Medical
- Inspection Date: 2018-04-02
- 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 1051621 - 2018-04-02](https://www.globalkeysolutions.net/api/records/fda_inspections/lincotek-medical/1bee55b3-a973-4fff-b44f-be8786d7e033/)

Company: https://www.globalkeysolutions.net/companies/lincotek-medical/cca8345c-bacd-4137-bf35-c65185228cbd

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