FDA Letter API

Battle Creek Equipment Co.

Letter data

Company
Battle Creek Equipment Co.
Recipient
David Underhill | President | Battle Creek Equipment Co. | 702 S. Reed Road | Fremont | , | IN | 46767-2098 | United States
Issue date
2019-07-09
Posted date
Not available
FDA office
Center for Device and Radiological Health
Subject
Not available
Product
Medical Devices
CMS ID
455012
Reference number
2015-DET-09
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 Battle Creek Equipment Co. MARCS-CMS 455012 — July 09, 2019 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: VIA UPS Reference #: 2015-DET-09 Product: Medical Devices Recipient: Recipient Name David Underhill Recipient Title President Battle Creek Equipment Co. 702 S. Reed Road Fremont , IN 46767-2098 United States Issuing Office: Center for Device and Radiological Health One Montvale Avenue Stoneham , MA 02180 United States Dear Mr. Underhill: The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter, 2015-DET-09 (CMS Case 455012), issued on April 3, 2015. Based on our evaluation, it appears that you have 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. Sincerely yours, /S/ Gina M. Brackett Director, Compliance Branch Office of Medical Device & Radiological Health Division-1 East Office of Regulatory Affairs U.S. Food and Drug Administration Content current as of: 07/09/2019 Regulated Product(s) Medical Devices