FDA Letter API

RX South DBA RX3 Compounding Pharmacy LLC

Letter data

Company
RX South DBA RX3 Compounding Pharmacy LLC
Recipient
Christopher K. Currin, R.Ph. | Co-Owner | RX South DBA RX3 Compounding Pharmacy LLC | 12230 Iron Bridge Rd. | Suite C | Chester | , | VA | 23831-1534 | United States
Issue date
2019-06-26
Posted date
Not available
FDA office
Center for Drug Evaluation and Research
Subject
Not available
Product
Drugs
CMS ID
440735
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 RX South DBA RX3 Compounding Pharmacy LLC MARCS-CMS 440735 — June 26, 2019 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Drugs Recipient: Recipient Name Christopher K. Currin, R.Ph. Recipient Title Co-Owner RX South DBA RX3 Compounding Pharmacy LLC 12230 Iron Bridge Rd. Suite C Chester , VA 23831-1534 United States Issuing Office: Center for Drug Evaluation and Research 10 Waterview Blvd. 3rd FL Parsippany , NJ 07054 United States (973) 331-4900 Dear Mr. Currin: The U.S. Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our warning letter dated October 23, 2014. Based on our evaluation, it appears that you have adequately addressed the violations contained in this warning letter. You are expected to take all necessary steps to ensure compliance with the Federal Food, Drug, and Cosmetic Act and FDA’s implementing regulations. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means. Sincerely, /S/ Craig Swanson Acting Program Division Director/District Director Office of Manufacturing Quality Operations Division I/New Jersey District Content current as of: 07/02/2019 Regulated Product(s) Drugs