# GlobalMed Inc. – FDA Inspection, Sep 6, 2013

Source: https://www.keypedia.com/records/fda_inspections/globalmed-inc/f665bf97-7a2a-40b8-a4e5-18d8f853d24a
Source feed: FDA_Inspections

> FDA inspection 847862 of GlobalMed Inc., September 06, 2013. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 847862
- Company Name: GlobalMed Inc.
- Inspection Date: 2013-09-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1206090 - 2023-04-27](https://www.keypedia.com/records/fda_inspections/globalmed-inc/a921c5ec-c16d-4d34-8f2a-aa62ddad09b1)
- [FDA Inspection 1064806 - 2018-09-07](https://www.keypedia.com/records/fda_inspections/globalmed-inc/413a917e-a888-4cd1-894a-8d5ec08a071c)

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