# FDA Inspection 1260276 - Aprios Custom Mfg - February 07, 2025

Source: https://www.keypedia.com/records/fda_inspections/aprios-custom-mfg/2fde461d-121e-4f89-8d7e-b10454321f35
Source feed: FDA_Inspections

> FDA inspection 1260276 of Aprios Custom Mfg, February 07, 2025. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260276
- Company Name: Aprios Custom Mfg
- Inspection Date: 2025-02-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1166867 - 2022-03-30
- [FDA Inspection 1049446 - 2018-04-04](https://www.keypedia.com/records/fda_inspections/aprios-custom-mfg/32f628a7-2cac-4e63-8895-6dfbb47753b9)
- FDA Inspection 862434 - 2014-01-07

## Related Officers

- [Investigator](https://www.keypedia.com/people/alicia-u-jacobo/5f75a995-c0df-4615-be88-d401df48ad26)

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