# CPG Sec. 398.325 Regulatory Actions Against Assemblers Noncompliant Diagnostic X-Ray Equipment - FDA Guidance Document

Source: https://www.keypedia.com/guidances/guidance-document/cpg-sec-398325-regulatory-actions-against-assemblers-noncompliant-diagnostic-x-ray-equipment/04bf4a60-dae5-4ccd-ac85-bf10f2e77151

> FDA guidance document: CPG Sec. 398.325 Regulatory Actions Against Assemblers Noncompliant Diagnostic X-Ray Equipment. Issue date: February 28, 2005. Get complete insights and analysis.

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## Details

- Title: CPG Sec. 398.325 Regulatory Actions Against Assemblers Noncompliant Diagnostic X-Ray Equipment
- Communication Type: Guidance Document
- Product Type: Medical Devices, Radiation-Emitting Products
- Office Name: Office of Regulatory Affairs
- Issue Date: 2005-02-28

## Related Documents

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- [CPG Sec. 398.375 Obligations of Factory-based Manufacturers and Assemblers of Diagnostic X-ray Equipment Under the Performance Standard for Diagnostic X-ray Equipment](https://www.keypedia.com/guidances/guidance-document/cpg-sec-398375-obligations-of-factory-based-manufacturers-and-assemblers-of-diagnostic-x-ray-equipment-under-the-performance-standard-for-diagnostic-x-ray-equipment/4419d9e5-51d6-47a5-b928-c1285739ffbd)
- [CPG Sec. 398.200 Hazardous Diagnostic X-ray Systems](https://www.keypedia.com/guidances/compliance-policy-guide-cpg/cpg-sec-398200-hazardous-diagnostic-x-ray-systems/6411b7a9-2b5d-4685-875f-59aec07506ee)
