# FDA Inspection 1043607 - Numedis Inc. - February 27, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/numedis-inc/dadea58b-283a-47e4-8dfe-40288075b4a8
Source feed: FDA_Inspections

> FDA Inspection 1043607 for Numedis Inc. on February 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1043607
- Company Name: Numedis Inc.
- Inspection Date: 2018-02-27
- 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 1043607 - 2018-02-27](https://www.globalkeysolutions.net/records/fda_inspections/numedis-inc/35fd0c39-2832-4c16-a349-85bb89143f13)
- [FDA Inspection 903411 - 2014-11-13](https://www.globalkeysolutions.net/records/fda_inspections/numedis-inc/f219b669-ebc8-472c-841a-59b513baf2e7)
- [FDA Inspection 782410 - 2012-05-21](https://www.globalkeysolutions.net/records/fda_inspections/numedis-inc/38edd5c4-a6fd-4899-a60e-558b7f9760f7)

Company: https://www.globalkeysolutions.net/companies/numedis-inc/5c9e24dc-00f8-417c-828e-3261f036c5a6

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