# AFP Manufacturing – FDA Inspection, Jun 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/afp-manufacturing/444d5260-fcd2-4fe5-8660-df7741562585
Source feed: FDA_Inspections

> FDA inspection 1094365 of AFP Manufacturing, June 27, 2019. Classification: No Action Indicated (NAI). 11 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094365
- Company Name: AFP Manufacturing
- Inspection Date: 2019-06-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 11

## Related Documents

- [FDA Inspection 1240105 - 2024-05-31](https://www.keypedia.com/records/fda_inspections/afp-manufacturing/9ec22951-c049-4260-a0aa-0e2f1ec5e1e4)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/miaja-umaedi/0a41661f-08bb-4523-ab09-b17e230068e0)
- [Issuing Officer](https://www.keypedia.com/people/trang-n-cox/436825b5-0375-4191-81b9-6e18b90d33af)

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