FDA Letter API

W & C dba The Apothecary

Letter data

Company
W & C dba The Apothecary
Recipient
Stephen G. Anderson, R. Ph. | Owner | W & C dba The Apothecary | 165 19th Street South | Suite 102 | Sartell | , | MN | 56377-2567 | United States
Issue date
2019-10-22
Posted date
Not available
FDA office
Division of Pharmaceutical Quality Operations III (PHRM3)
Subject
Not available
Product
Drugs
CMS ID
508183
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 W & C dba The Apothecary MARCS-CMS 508183 — October 22, 2019 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: UPS Next Day Product: Drugs Recipient: Recipient Name Stephen G. Anderson, R. Ph. Recipient Title Owner W & C dba The Apothecary 165 19th Street South Suite 102 Sartell , MN 56377-2567 United States Issuing Office: Division of Pharmaceutical Quality Operations III (PHRM3) 300 River Place Suite 5900 Detroit , MI 48207 United States (313) 393-8100 Dear Mr. Anderson: 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 July 20, 2017, (Case #508183). We acknowledge that your firm no longer produces sterile drug products. 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 assure 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/ Nicholas F. Lyons Director Compliance Branch Division of Pharmaceutical Quality Operations III Content current as of: 10/30/2019 Regulated Product(s) Drugs