# FDA Inspection 1103588 - RevMedx, Inc. - September 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/revmedx-inc/969415ed-d4b1-46ec-abae-4d251bbb4f2a
Source feed: FDA_Inspections

> FDA Inspection 1103588 for RevMedx, Inc. on September 26, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1103588
- Company Name: RevMedx, Inc.
- Inspection Date: 2019-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1103588 - 2019-09-26](https://www.keypedia.com/records/fda_inspections/revmedx-inc/ea1d0698-d7fc-48e8-b306-cba929479130)
- [FDA Inspection 949120 - 2015-11-23](https://www.keypedia.com/records/fda_inspections/revmedx-inc/ad65a415-edf7-4ee7-b40c-9eb7861b44f5)
- [FDA Inspection 949120 - 2015-11-23](https://www.keypedia.com/records/fda_inspections/revmedx-inc/4a81fa1c-becb-4bdd-99e3-531a23274270)

Company: https://www.keypedia.com/companies/revmedx-inc/de0ba5ed-9e58-49f5-8d13-6554ec8610fc

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