Sterling Medical Devices & RBC Medical Innovations are combining to create Vantage MedTech! Meet RBC
Contact Us
Close Form

Interested in learning more about how we can work together in your current or next medical device design project?

Just fill out this form and we’ll be in touch!

  • This field is for validation purposes and should be left unchanged.

Wherever you are in your product development lifecycle,
Sterling can help.

P: 201-877-5682
F: 201-301-9169
info@sterlingmedicaldevices.com

FDA Warning Letter Support

Has your company received an FDA warning letter? The FDA will issue a warning letter notifying you if they find a violation or non-compliance regarding your device. These letters indicate serious issues and require a prompt response. Failure to respond can lead to fines, injunctions, product seizure or recalls, and more. Common issues that result in FDA warning letters include:

  • False or inadequate labeling
  • False or incorrect instructions for use
  • False or unsubstantiated medical claims
  • Medical claims for an unapproved product
  • Failure to obtain a marketing authorization from FDA
  • Incorrect or undocumented design controls or manufacturing processes
  • Non-compliance with written procedures
  • Misbranded or adulterated products
Contact Us

The FDA warning letter will state corrective actions required, a timeline to complete them, as well as the consequences of failing to comply with the letter. You have a limited time to respond to the letter and it is critical that your response is satisfactory. Sterling’s regulatory experts have helped countless companies with FDA warning letter responses. We’ll help you quickly respond to the letter and address the listed violations.

FDA Warning Letter Support:

We will accompany you through the complexities of the FDA warning letter, ensuring you act quickly and proactively to resolve the regulatory issues in question.

With our Regulatory Support Services, we’ll partner with you to:

  • Analyze the contents of the FDA warning letter
  • Draft a response to the FDA
  • Develop a plan to address the issues
  • Create a timeline for implementation
  • Lead or assist in the implementation of the plan
  • Field questions from you or the FDA during corrective action activities

Turn it over to Sterling

With our Regulatory Support Services, you get a partner with decades of experience helping clients achieve and maintain regulatory compliance. Let us help you keep your device on the market, and rest easy knowing you’re in capable and experienced hands.

To learn more about how Sterling can help you address FDA warning letters, fill out the form above.

Share this!

Resources

Doctor on phone communicating with patient

September 26, 2023

Avoiding Pitfalls with Smartphone Medical Devices

Smartphones are everywhere. They help us pay our bills, keep our calendars, connect us to our colleagues and loved ones, save our most precious memories, and more. But did you know the value of...
Read More >
View More Blogs
5 Mistakes Medical Device Startups Make

February 18, 2021

5 Mistakes Medical Device Startups Make

Startups are the lifeblood of medical device innovation. Without universities researching ways to solve pressing healthcare problems or doctors with experience in a particular field who have an idea to develop a prototype medical device that could help patients, the future technologies needed to help save lives wouldn't happen. But the long, arduous road through the FDA submission process to get market approval can take a long time and cost a lot of money without help. Sterling Medical Devices has been helping startups through the FDA approval process since 1998 without ever having a submission rejected.
Read More >
View More Videos

April 5, 2023

Sterling Medical Devices Creates Controller to Groundbreaking New Multi-Pump Mechanical Circulatory Support Device

Controller to Power Groundbreaking New Multi-Pump Mechanical Circulatory Support Device Medical Device Need A controller for an implantable heart pump that...
Read More >
View More Case Studies

Need help with your medical device?

Let Sterling Medical Devices show how to bring your idea from concept to prototype to
FDA/CE approval with a free custom project analysis.
Request Free Analysis