FDA Letter API

Lydia Co Ltd.

Letter data

Company
Lydia Co Ltd.
Recipient
Ho Dong Yang | Lydia Co Ltd. | 102, Dongguk-ro | ILsandong-gu | Goyang-si | 10325 | South Korea | onbix@naver.com
Issue date
2023-08-18
Posted date
Not available
FDA office
Center for Drug Evaluation and Research | CDER
Subject
Not available
Product
Drugs
CMS ID
659646
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 Lydia Co Ltd. MARCS-CMS 659646 — August 18, 2023 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Drugs Recipient: Recipient Name Ho Dong Yang Lydia Co Ltd. 102, Dongguk-ro ILsandong-gu Goyang-si 10325 South Korea onbix@naver.com Issuing Office: Center for Drug Evaluation and Research | CDER United States Dear Ho Dong Yang: The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter # 2575. Based on our evaluation, it appears that you have addressed the violations contained in the warning letter and corrected the data discrepancies between labeling and electronic listing files, thus this warning letter is closed. Future FDA regulatory activities will further assess the adequacy and sustainability of these corrections. 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. If this product is reintroduced in U.S. commercial distribution, FDA expects that all previous errors are corrected. The Agency expects you and your firm to maintain compliance and to continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means. Sincerely, /S/ Tina Smith Acting Director, Office of Unapproved Drugs & Labeling Compliance Center for Drug Evaluation and Research Office of Compliance U.S. Food and Drug Administration Content current as of: 08/23/2023 Regulated Product(s) Drugs