FDA Letter API

Soulaire Corporation

Letter data

Company
Soulaire Corporation
Recipient
Morad Soulati | Chief Executive Officer (CEO) | Soulaire Corporation | 1934 14th Street, Unit A | Santa Monica | , | CA | 90404 | United States | mo@soulaire.com
Issue date
2026-08-24
Posted date
Not available
FDA office
Center for Devices and Radiological Health
Subject
Not available
Product
Medical Devices
CMS ID
675069
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

FDA closeout letter

Full source text

CLOSEOUT LETTER Soulaire Corporation MARCS-CMS 675069 — August 24, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: VIA Electronic Mail Product: Medical Devices Recipient: Recipient Name Morad Soulati Recipient Title Chief Executive Officer (CEO) Soulaire Corporation 1934 14th Street, Unit A Santa Monica , CA 90404 United States mo@soulaire.com Issuing Office: Center for Devices and Radiological Health United States Secondary Issuing Offices United States Dear Mr. Soulati: The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter (CMS # 675069, dated January 29, 2024). 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, /S/ For Barbara C. Marsden Director Office of Regulatory Programs Office of Product Evaluation and Quality Center for Devices and Radiological Health Content current as of: 08/31/2026 Regulated Product(s) Medical Devices