ANSWERED ON THIS PAGE:
- What is an FDA Form 483?
- What are the next steps after getting an FDA Form 483?
- What is an FDA Warning Letter?
- How can you recover from an FDA 483 or Warning Letter?
No medical device or IVD manufacturer wants to receive a Form 483 or Warning Letter from the US Food and Drug Administration (FDA). The FDA Form 483 is officially called a "Notice of Inspectional Observations," commonly referred to simply as a "483." The 483 is issued at the end of an on-site inspection if the FDA field investigator observed deficiencies in your quality system or conditions that violate the Food, Drug, or Cosmetic Act.
You got a US FDA form 483 – now what?
The field inspector will submit the final 483 to his/her superiors; if the findings are serious enough, or if the response to the 483 that you submit is deemed insufficient, an FDA Warning Letter may be issued to your firm. A Warning Letter is the FDA's advisory notice that you have significantly violated FDA regulations. It will identify the violation(s), and make it clear that you must correct the problems and inform the FDA of your specific plans for correction of the problem, including actions to prevent it or a similar problem from re-occurring. The FDA will check to determine whether your corrections are adequate.
How to respond to a Form 483 or warning letter
You must respond to the 483 or a Warning Letter promptly and identify your course of action to correct the findings within the FDA's specified timeframe. A detailed response to each observation or violation noted is also required. The quality and promptness of your response to this letter are extremely important.
Emergo can help you respond to an FDA Form 483 or warning letter
Emergo can assist you in preparing an effective response to an FDA Form 483 and Warning Letter. We can provide you with direction to bring your quality system into full compliance with the regulations. As part of our services, we will:
- Analyze the findings of the FDA Form 483 and/or Warning Letter.
- Suggest an appropriate timeline to satisfy the FDA.
- Assist your company in charting a course of action.
- Propose "Corrective Actions" to be made to your quality system.
- Assist in implementing corrective actions in response to FDA Form 483.
- Be available to answer all questions from you or the FDA during your efforts to correct the noted deficiencies or violations.
Emergo has worked with numerous medical device and IVD companies to formulate proper responses to FDA 483 and Warning Letters.
How can we avoid receiving a Form 483 or Warning Letter?
The best way to minimize your chances of receiving a Form 483 is to always be "inspection ready." In other words, your quality management system should comply with US FDA 21 CFR Part 820 (Quality System Regulation) at all times because the FDA conducts random QSR audits with very little notice. Conduct regular internal audits of your QMS and learn what to expect from an FDA QSR inspection. Emergo can help with quality management system implementation and perform audits.
What if the Form 483 or Warning Letter results in a recall?
Emergo offers a range of post-market consulting services, including surveillance, vigilance, Field Safety Corrective Actions (FSCAs), and recalls. If you choose to withdraw your product from the US market in this situation, we can also help you design an exit strategy.