# FDA Inspection 1203161 - VentureMed Group, Inc. - April 05, 2023

Source: https://www.keypedia.com/records/fda_inspections/venturemed-group-inc/c6de12d8-de58-4133-9d4c-186d00dbba7a
Source feed: FDA_Inspections

> FDA Inspection 1203161 for VentureMed Group, Inc. on April 05, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1203161
- Company Name: VentureMed Group, Inc.
- Inspection Date: 2023-04-05
- 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 1203161 - 2023-04-05](https://www.keypedia.com/records/fda_inspections/venturemed-group-inc/6e3b7c3f-b826-470f-b3e3-89de8558667e)
- [FDA Inspection 1089214 - 2019-04-18](https://www.keypedia.com/records/fda_inspections/venturemed-group-inc/5590c357-8b4b-480f-a38b-d487d39c9d3d)
- [FDA Inspection 1089214 - 2019-04-18](https://www.keypedia.com/records/fda_inspections/venturemed-group-inc/2f4c5004-392c-4fef-8ce2-4b603a79ba4a)

Company: https://www.keypedia.com/companies/venturemed-group-inc/51c31148-f49a-4186-a829-b0dcf53a40bd

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