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FDA Cancels Shivnath Ayurveda's Licence After ANiS Complaint

FDA Cancels Shivnath Ayurveda's Licence After ANiS Complaint
Nashik: FDA Permanently Cancels Shivnath Ayurveda's Manufacturing Licence Following ANiS Complaint · freepressjournal.in

The Food and Drug Administration (FDA) in Nashik, Maharashtra, has permanently cancelled the manufacturing licence of Shivnath Ayurveda Product Company.

This decision came after the Maharashtra Andhashraddha Nirmoolan Samiti (ANiS) filed a complaint against the company's owner, Dr. Mohan Puri, alleging illegal drug manufacturing and quackery.

The FDA inspected the company's facility in Jaigaon and found serious violations of pharmaceutical standards and the Drugs and Cosmetics Act.

After a hearing, the FDA decided to permanently cancel the company's licence.

Dr. Puri is also alleged to be associated with Rajendra Gadge Baba, a self-styled godman, and is suspected of supplying unapproved medicines.

Key facts

Company Name
Shivnath Ayurveda Product Company
Owner
Dr. Mohan Puri
Location
Jaigaon, Sinnar taluka, Nashik
Complaint Filed By
Maharashtra Andhashraddha Nirmoolan Samiti (ANiS)
Allegations
Illegal drug manufacturing and quackery
Action Taken
Permanent cancellation of manufacturing licence
Date of Decision
June 30, 2026
Key Figures Involved
Advocate Ranjana Pagar-Gawande, Dr. T. R. Gorane, Prof. Dr. Sudesh Ghoderao, Krishna Chandgude

Sources

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