This survey is being conducted by the Medical Device Single Audit Program (MDSAP) development team to determine if MDSAP processes are meeting expectations. All comments will be considered and could be used to revise MDSAP processes and procedures. All answers to the questions below will remain anonymous and confidential and will be disclosed in aggregated form for subsequent analysis.

We appreciate your participation in this survey. It should only take about 5 minutes to complete.

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* 1. Was the audit duration appropriate?

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* 2. How effective was the training to conduct and document the audit?

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* 3. How effective were the tools available to conduct and document the audit?

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* 4. Did the RA observers respect their roles?

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* 5. Are there any areas that require additional guidance/ interpretation from the regulatory authorities (RAs)?

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* 6. How well did it work with the audit model?

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* 7. Did you have problems with the report template?

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* 8. Please use this space to share any additional comments you have regarding the auditing process.

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