# Medical Device Reporting for User Facilities - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/medical-device-reporting-for-user-facilities/b0da1f94-9b65-49d9-a1ac-e1c781b3107d

> FDA guidance document: Medical Device Reporting for User Facilities. Issue date: April 01, 1996. Get complete insights and analysis.

---

## Details

- Title: Medical Device Reporting for User Facilities
- Communication Type: Guidance Document
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
- Issue Date: 1996-04-01
- Last Changed: 2020-03-18
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2020-D-0957">FDA-2020-D-0957</a>

## Related Documents

- [Guidance on Medical Device Patient Labeling:  Final Guidance for Industry and FDA Staff](https://www.globalkeysolutions.net/guidances/guidance-document/guidance-on-medical-device-patient-labeling-final-guidance-for-industry-and-fda-staff/2d0df546-e5c9-4546-a856-88c928b342fd)
- [Quality Control Guide for Sunlamp Products (FDA 88-8234)](https://www.globalkeysolutions.net/guidances/guidance-document/quality-control-guide-for-sunlamp-products-fda-88-8234/b3011663-c501-41b1-aa76-7faad0ddab28)
- [National Uniformity for Nonpresciption Drugs - Ingredient Listing for OTC Drugs](https://www.globalkeysolutions.net/guidances/guidance-document/national-uniformity-for-nonpresciption-drugs-ingredient-listing-for-otc-drugs/9d832005-d340-46af-95c2-1e3fa3b3ab8b)