FDA Letter API

Shenzhen Sunell Technology Corporation

Letter data

Company
Shenzhen Sunell Technology Corporation
Recipient
Ann Wu | Chief Executive Officer | Shenzhen Sunell Technology Corporation | 4 Aerospace Micromoto Bldg. 2 Floor 5 | Shenzhen | China | annwu@sunellsecurity.com
Issue date
2023-07-20
Posted date
Not available
FDA office
Center for Devices and Radiological Health
Subject
Not available
Product
Medical Devices
CMS ID
613563
Reference number
Not available
FEI
Not available
Inspection dates
Not available

Normalized citations

21 CFR: None found

21 U.S.C.: None found

Related FDA links

No related FDA letter link is present in the source index.

Full source text

CLOSEOUT LETTER Shenzhen Sunell Technology Corporation MARCS-CMS 613563 — July 20, 2023 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Medical Devices Recipient: Recipient Name Ann Wu Recipient Title Chief Executive Officer Shenzhen Sunell Technology Corporation 4 Aerospace Micromoto Bldg. 2 Floor 5 Shenzhen China annwu@sunellsecurity.com Issuing Office: Center for Devices and Radiological Health United States Dear Ann Wu: The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter (CMS # 613563, dated March 4, 2021). Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed in the future. Sincerely yours, /S/ Courtney H. Lias, Ph.D. Office Director OHT3: Office of GastroRenal, ObGyn, General Hospital and Urology Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Content current as of: 07/27/2023 Regulated Product(s) Medical Devices