# FDA Inspection 1099578 - Gi Supply - December 18, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/gi-supply/3f41c00a-a6cd-4909-8f6c-5eecdae42325
Source feed: FDA_Inspections

> FDA Inspection 1099578 for Gi Supply on December 18, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099578
- Company Name: Gi Supply
- Inspection Date: 2018-12-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 893107 - 2014-08-26](https://www.globalkeysolutions.net/records/fda_inspections/gi-supply/a59fd663-d674-49d2-bad6-a1c9fa062a7d)
- [FDA Inspection 658683 - 2010-04-21](https://www.globalkeysolutions.net/records/fda_inspections/gi-supply/8ab7b797-b12a-4448-9986-4b463315560c)

Company: https://www.globalkeysolutions.net/companies/gi-supply/cae73705-0bf5-4751-88fe-87f4fd38c436

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