FDA Letter API

Indus Medicare Limited

Letter data

Company
Indus Medicare Limited
Recipient
Pingle Janardhan Reddy | Managing Director | Indus Medicare Limited | Sy No. 129, NH-44, Ramaipally Village | Manoharabad Mandal | Medak District | 502336 | Telangana | India
Issue date
2021-02-17
Posted date
Not available
FDA office
Center for Devices and Radiological Health
Subject
Not available
Product
Medical Devices
CMS ID
606159
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 Indus Medicare Limited MARCS-CMS 606159 — February 17, 2021 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Medical Devices Recipient: Recipient Name Pingle Janardhan Reddy Recipient Title Managing Director Indus Medicare Limited Sy No. 129, NH-44, Ramaipally Village Manoharabad Mandal Medak District 502336 Telangana India Issuing Office: Center for Devices and Radiological Health United States Dear Pingle Janardhan Reddy: The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter (CMS #606159, dated May 4, 2020). Based on our evaluation, it appears that you have addressed the violation(s) contained in this Warning Letter. Future FDA inspections and 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. The Agency expects you and your firm to maintain compliance and will 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 yours, /S/ Sharon M. Andrews Director DHT3B: Division of Reproductive, Gynecology and Urology Devices OHT3: Office of GastroRenal, ObGyn, General Hospital and Urology Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health CC: Bill Taffs Eagle TWE Inc., 4761 Hugh Howell Road, Unit M Tucker, Georgia 30084 Email: Bill@Eagletwe.com Content current as of: 02/14/2022 Regulated Product(s) Medical Devices