# FDA Inspection 1117890 - InteloMed, Inc. - January 15, 2020

Source: https://www.keypedia.com/records/fda_inspections/intelomed-inc/d037973c-1d3e-47de-a485-8465db28ae5e
Source feed: FDA_Inspections

> FDA Inspection 1117890 for InteloMed, Inc. on January 15, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1117890
- Company Name: InteloMed, Inc.
- Inspection Date: 2020-01-15
- 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 1117890 - 2020-01-15](https://www.keypedia.com/records/fda_inspections/intelomed-inc/5e977d68-82b7-4c26-b4eb-be055988842b)
- [FDA Inspection 1012237 - 2017-02-28](https://www.keypedia.com/records/fda_inspections/intelomed-inc/544311b4-d4fb-4d21-a4b5-1dcbbebe1358)
- [FDA Inspection 1012237 - 2017-02-28](https://www.keypedia.com/records/fda_inspections/intelomed-inc/195992c4-8eae-4ec9-8cde-61a2f1314d50)

Company: https://www.keypedia.com/companies/intelomed-inc/f6db03ca-d4f1-4451-b705-e9de0458dafd

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