# FDA Inspection 1080808 - Lochness Medical, Inc. - February 26, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/lochness-medical-inc/038cdd05-8292-44c6-b924-1dd7d8f0d359
Source feed: FDA_Inspections

> FDA Inspection 1080808 for Lochness Medical, Inc. on February 26, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1080808
- Company Name: Lochness Medical, Inc.
- Inspection Date: 2019-02-26
- 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 1080808 - 2019-02-26](https://www.globalkeysolutions.net/records/fda_inspections/lochness-medical-inc/f22df533-f649-4b1a-9d4c-56f8101b056d)

Company: https://www.globalkeysolutions.net/companies/lochness-medical-inc/9f6f48fa-c785-42eb-9286-e3337fb470ab

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