Inspection Readiness - Part Three

Recovering from an FDA inspection

Your inspection is over, but that’s not the end if unacceptable conditions have been observed. It’s the beginning of a final phase that must be appropriately managed to bring your company and device into compliance. 

Inspection observations and citations

Observations are listed on U.S. Food and Drug Administration (FDA) Form 483 in order of severity, as determined by the inspector. Each observation includes a citation of the law, regulation, or Act that applies to each particular finding and a statement of the specific conditions noted during the inspection.

Data from the FDA shows that 422 Form 483s were issued to device manufacturers between October 1, 2019, and September 30, 2020 (FY 2020).  Reasons for receiving a 483 are varied but frequently include:

• Failure to investigate device, packaging, or labeling flaws
• Failure to provide access to management or SMEs
• Failure to provide adequate supplier data
• Failure to submit timely Medical Device Reporting (MDR)
• Failure to validate automation software for its intended use
• Lack of design history files or design validation
• Lack of documentation, reports, records, or files
• Lack of maintenance schedules
• Lack of training, quality, process control, or environmental procedures

Form 483 responses

Form 483s are provided to company management at the end of the inspection. The inspector recites the observations and discusses their significance to ensure that each citation is fully understood. 

Companies are expected to respond to the 483s in writing, with a comprehensive outline of corrective actions for each citation. You should list citations in the order of severity, beginning with the most severe. 

Responses should be submitted within 15 days after receiving a 483. If time allows, you may wish to engage legal counsel to review your answers. 

Corrective actions should be put in place as soon as possible. It is also wise to review processes and procedures not cited to take proactive measures before the next inspection. 

Warning letters

FDA warning letters are much more severe than Form 483 in that they address critical violations with the potential to disrupt or halt business. A warning letter provides directions for a thorough response and a firm deadline for receipt of said response.

Reasons for receiving a warning letter are varied. The FDA warning letter database lists several recurring subjects including, but not limited to:

• False or misleading claims
• Incomplete quality system regulation (QSR)
• Investigational device exemptions
• Lack of premarket approval (PMA) inspection
• Nonconformance with current good manufacturing practice (cGMP) guidelines
• Unapproved, adulterated, or misbranded products

Failure to expedite corrective actions, as outlined in your response, can result in fines, criminal complaints, or orders to stop production. 

Consent decrees

A consent decree comes down after recurrent nonconformance with cGMP guidelines, as noted in Form 483 observations and subsequent warning letters. It is a legal agreement enforced by the U.S. Department of Justice (DOJ). This action impacts all business areas with heavy financial penalties, remediation costs, dropped sales, lower stock value, and a tarnished reputation.

The Food and Drug Law Institute outlines the components of a consent decree as ordered under the Federal Food, Drug, and Cosmetic Act (FDCA). While the specifics will vary, consent decrees typically involve:

• Naming of individual defendants
• Injunctive provisions regarding the resumption of operations
• Engagement of an independent auditor at the company’s cost
• Agreed upon schedule of periodic audits “Letter shutdown” provision which allows the government to close business operations
• Liquidated damages paid to the government by the day, by the violation, and by the retail value
• Notification of any change in ownership or named defendants
• Length of the decree and its dissolution under court order

The government may also seek disgorgement and restitution. However, this controversial action has been challenged before the Supreme Court. 

Expert support is available for your inspection readiness needs. Learn how SRG can help. Contact us at USMarketing.