FDA Letter API

Procter & Gamble Manufactura S. de R.L. de C.V.

Letter data

Company
Procter & Gamble Manufactura S. de R.L. de C.V.
Recipient
Maria Petry | Procter & Gamble Manufactura S. de R.L. de C.V. | 8700 Mason-Montgomery Road | Mason | , | OH | 45040-9462 | United States
Issue date
2023-03-27
Posted date
Not available
FDA office
Center for Drug Evaluation and Research | CDER
Subject
Not available
Product
Drugs
CMS ID
650837
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 Procter & Gamble Manufactura S. de R.L. de C.V. MARCS-CMS 650837 — March 27, 2023 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Drugs Recipient: Recipient Name Maria Petry Procter & Gamble Manufactura S. de R.L. de C.V. 8700 Mason-Montgomery Road Mason , OH 45040-9462 United States Issuing Office: Center for Drug Evaluation and Research | CDER United States Dear Ms. Petrey: The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter # 2496. Based on our evaluation, you have discontinued the product listing by adding an end marketing date to the drug listing data thus the 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: 03/31/2023 Regulated Product(s) Drugs