# FDA Inspection 1094365 - AFP Manufacturing - June 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/afp-manufacturing/0ee3ef42-927e-45af-b80d-07b805175c02
Source feed: FDA_Inspections

> FDA Inspection 1094365 for AFP Manufacturing on June 27, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094365
- Company Name: AFP Manufacturing
- Inspection Date: 2019-06-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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