# FDA Inspection 1049446 - Aprios Custom Mfg - April 04, 2018

Source: https://www.keypedia.com/records/fda_inspections/aprios-custom-mfg/32f628a7-2cac-4e63-8895-6dfbb47753b9
Source feed: FDA_Inspections

> FDA inspection 1049446 of Aprios Custom Mfg, April 04, 2018. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1049446
- Company Name: Aprios Custom Mfg
- Inspection Date: 2018-04-04
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1260276 - 2025-02-07](https://www.keypedia.com/records/fda_inspections/aprios-custom-mfg/b13de0ae-0048-471a-bb57-de8080921aeb)
- FDA Inspection 1166867 - 2022-03-30
- FDA Inspection 862434 - 2014-01-07

Company: https://www.keypedia.com/companies/aprios-custom-mfg/07c8421d-293c-4a7f-bc8e-61789ab63848

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