# FDA Inspection 1167290 - BELLFX - March 31, 2022

Source: https://www.keypedia.com/records/fda_inspections/bellfx/83d87b88-9b3f-48b4-9838-020d4512dcd5
Source feed: FDA_Inspections

> FDA Inspection 1167290 for BELLFX on March 31, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1167290
- Company Name: BELLFX
- Inspection Date: 2022-03-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/bellfx/b1cd44d3-c3ed-47bb-941c-31e3aa297f96

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