FDA Letter API

Ocular Therapeutix Inc.

Letter data

Company
Ocular Therapeutix Inc.
Recipient
Ms. Nicole Oliynyk | Senior Director, Regulatory Affairs | Ocular Therapeutix Inc. | 24 Crosby Drive | Bedford | , | MA | 01730 | United States
Issue date
2020-09-02
Posted date
Not available
FDA office
Center for Devices and Radiological Health
Subject
Not available
Product
Medical Devices
CMS ID
564663
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 Ocular Therapeutix Inc. MARCS-CMS 564663 — September 02, 2020 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Medical Devices Recipient: Recipient Name Ms. Nicole Oliynyk Recipient Title Senior Director, Regulatory Affairs Ocular Therapeutix Inc. 24 Crosby Drive Bedford , MA 01730 United States Issuing Office: Center for Devices and Radiological Health United States Dear Ms. Oliynyk: The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter (CMS # 564663, dated October 18, 2018). 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/ for Malvina B. Eydelman, M.D. Director Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Content current as of: 03/02/2021 Regulated Product(s) Medical Devices