# FDA Inspection 1206090 - GlobalMed Inc. - April 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/globalmed-inc/a921c5ec-c16d-4d34-8f2a-aa62ddad09b1
Source feed: FDA_Inspections

> FDA Inspection 1206090 for GlobalMed Inc. on April 27, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1206090
- Company Name: GlobalMed Inc.
- Inspection Date: 2023-04-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1206090 - 2023-04-27](https://www.keypedia.com/records/fda_inspections/globalmed-inc/09fa5d9e-6847-4510-87d9-6237b82a97e0)
- [FDA Inspection 847862 - 2013-09-06](https://www.keypedia.com/records/fda_inspections/globalmed-inc/f665bf97-7a2a-40b8-a4e5-18d8f853d24a)

Company: https://www.keypedia.com/companies/globalmed-inc/2434eae5-2b49-45ec-a153-b621e5819e3c

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