Recipient NameRandel Woodgrift
Recipient TitleSenior Vice President
15900 Valley View Court
Sylmar, CA 91342
- Issuing Office:
- Medical Device & Radiological Health Operations Division 3/West
Dear Mr. Woodgrift:
The Food and Drug Administration has completed evaluation of your firm’s corrective actions in response to our Warning Letter (CMS #519686, April 12, 2017). Based on our evaluation, it appears that your firm has addressed the violations 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.
Jessica Mu, Director of Compliance
Medical Device & Radiological Health Operations