| Warning Letters | Regulatory Action Reports | OpenFDA: CAERs | Recalls |
This chart indicates the total number of observations (broken down by 21 CFR 111 subpart and FDA fiscal year) found during FDA inspections of dietary supplement companies and includes adverse event reporting data ('subpart X'). You can choose a specific year or drill down on a subpart by clicking the description.
DISCLAIMER: These charts are compiled from FDA data. The author does not guarantee that all information provided is accurate and complete, as FDA may redact certain information from the published datasets. Please confirm your conclusions by checking at the FDA web site: Inspection Classifications and Inspection Observations or make a FOI request to FDA. I will be glad to make a FOI request on your behalf, please contact me.
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