# Medical Device Reports; Reports of Corrections and Removals; Establishment Registration and Device Listing: Premarket Approval Supplements; Quality System Regulation; Importation of Electronic Products; Technical Amendment
> **Food and Drug Administration** · Final rule; technical amendment. · Published 2004-03-10 · 69 FR 11310
## Document
- **Document number:** 04-5302
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 69 FR 11310
- **CFR reference:** 21 CFR 803
- **Publication date:** 2004-03-10
## Abstract

The Food and Drug Administration (FDA) is correcting certain regulations in 21 CFR parts 803, 806, 807, 814, 820, and 1005. This rule corrects some inadvertent typographical errors and some technical errors, and it is intended to improve the accuracy of the agency's regulations.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2004/03/10/04-5302/medical-device-reports-reports-of-corrections-and-removals-establishment-registration-and-device)
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