FDA Letter API

Rite Aid Corporation

Letter data

Company
Rite Aid Corporation
Recipient
Elizabeth Hanlon | Rite Aid Corporation | 200 Newberry Commons | Etters | , | PA | 17319 | United States
Issue date
2022-12-20
Posted date
Not available
FDA office
Center for Drug Evaluation and Research | CDER
Subject
Not available
Product
Drugs
CMS ID
643207
Reference number
WL 2277
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 Rite Aid Corporation MARCS-CMS 643207 — December 20, 2022 More Warning Letters Warning Letters About Warning and Close-Out Letters Reference #: WL 2277 Product: Drugs Recipient: Recipient Name Elizabeth Hanlon Rite Aid Corporation 200 Newberry Commons Etters , PA 17319 United States Issuing Office: Center for Drug Evaluation and Research | CDER United States Dear Ms. Hanlon: The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter # 2277. Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter and corrected the data deficiencies. We have received an updated listing SPL with the correct list of active ingredients and an updated labeler code request SPL with the updated contact information. 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 ensure 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 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/ Carolyn E. Becker, JD Director, Office of Unapproved Drugs & Labeling Compliance Office of Compliance Center for Drug Evaluation and Research U.S. Food and Drug Administration Content current as of: 12/27/2022 Regulated Product(s) Drugs