The answer is: The FDA assesses the relationship, if any, between a product or ingredient and the reported adverse event.
The option above describes how the FDA investigates reports of harmful cases after consuming certain product.
The rest of the alternatives are incorrect because the second refers to obstacles that impede the FDA access to medical records, the third option examines the cause of the event, and the last one makes reference to how seriously the FDA takes every case.
I would say read closely and highlight any important details. If the textbook belongs to the school and you're not allowed to write on it, take some notes and write down the important details on a different piece of paper.
Answer:
A
Explanation:
Nobody will ever really understand anyone else's story because nobody knows what anyone else is going through.
