FDA Letter API

Global Calcium House 1

Letter data

Company
Global Calcium House 1
Recipient
Mr. Sahil Vaz | Chief Executive Officer (CEO)/ Managing Director | Global Calcium House 1 | Global Calcium Pvt. Limited | Hundred Feet Road | Koramangala Bangalore | 560095 | India
Issue date
2026-07-30
Posted date
Not available
FDA office
Center for Drug Evaluation and Research (CDER)
Subject
Not available
Product
Drugs
CMS ID
692000
Reference number
Not available
FEI
3004094136
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 Global Calcium House 1 MARCS-CMS 692000 — July 30, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Reference #: FEI 3004094136 Product: Drugs Recipient: Recipient Name Mr. Sahil Vaz Recipient Title Chief Executive Officer (CEO)/ Managing Director Global Calcium House 1 Global Calcium Pvt. Limited Hundred Feet Road Koramangala Bangalore 560095 India Issuing Office: Center for Drug Evaluation and Research (CDER) United States Secondary Issuing Offices United States Dear Mr. Vaz: The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-25-30 dated January 16, 2025. Based on our evaluation, it appears that you have addressed the deviations 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 FDA 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 deviations be observed during a subsequent inspection or through other means. Sincerely, /S/ Matthew Jensen Compliance Officer Division of Drug Quality I Content current as of: 07/30/2026 Regulated Product(s) Drugs