# FDA Inspection 1232932 - Phelcom Technologies SA - March 14, 2024

Source: https://www.keypedia.com/records/fda_inspections/phelcom-technologies-sa/1dc9a0ba-cb20-4681-9638-1499a8dce146
Source feed: FDA_Inspections

> FDA inspection 1232932 of Phelcom Technologies SA, March 14, 2024. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1232932
- Company Name: Phelcom Technologies SA
- Inspection Date: 2024-03-14
- 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: 8

## Related Officers

- [Company Rep](https://www.keypedia.com/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

Company: https://www.keypedia.com/companies/phelcom-technologies-sa/057fee8a-49e7-4b60-92ac-f7693b5f7aa5

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