# AFP Manufacturing – FDA Inspection, May 31, 2024

Source: https://www.keypedia.com/records/fda_inspections/afp-manufacturing/9ec22951-c049-4260-a0aa-0e2f1ec5e1e4
Source feed: FDA_Inspections

> FDA inspection 1240105 of AFP Manufacturing, May 31, 2024. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1240105
- Company Name: AFP Manufacturing
- Inspection Date: 2024-05-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1094365 - 2019-06-27](https://www.keypedia.com/records/fda_inspections/afp-manufacturing/444d5260-fcd2-4fe5-8660-df7741562585)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/ronald-ifraimov/b4ce8b79-3fa2-4862-b7a4-68e14e45d87a)

Company: https://www.keypedia.com/companies/afp-manufacturing/29ad525f-9746-46b0-b299-4dce540c6ab1

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