# FDA Inspection 1280318 - Precision Adm - July 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/precision-adm/077c6ef9-4f99-46b2-8901-99d460f6c4d3
Source feed: FDA_Inspections

> FDA Inspection 1280318 for Precision Adm on July 10, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280318
- Company Name: Precision Adm
- Inspection Date: 2025-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1280318 - 2025-07-10](https://www.keypedia.com/records/fda_inspections/precision-adm/4dd49573-f1f4-4696-a9ce-e882332fe5a8)

Company: https://www.keypedia.com/companies/precision-adm/5f591b38-3353-4433-84f5-fbe1e454df89

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