Companies should have a plan in place for the event product is sampled, whether that is in the market, or during an inspection. If FDA samples product or the environment during an facility inspection, consider:
- Holding product.
- Stopping production and conducting a complete sanitation.
- Pulling duplicate samples and having them tested.
One of the difficulties is the delay that can occur with FDA getting back to a facility with results. The longer the period, the more exposure in terms of extent of product distribution.
A proactive approach is always best - developing and implementing a sampling program to understand and control potential risks.
FDA Website - Sampling
Sampling to Protect the Food Supply
The FDA Food Safety Modernization Act is based on preventing problems before they happen, rather than solely responding to outbreaks of foodborne illness. But in order to develop prevention-based systems, you need data and other information to help identify hazards that need to be addressed and minimized.
That is why sampling is an important part of this preventive approach and why the FDA is developing a new microbiological surveillance sampling model designed to identify patterns that may help predict and prevent future contamination by disease-causing bacteria.