Glossary
Sherry K Markwell
FDA Investigator Details
Sherry K Markwell
Visit Investigator ProfileInvestigation Details
Last Issued Date
December 29, 2015
Conversion Rate
0
% Conversion
No. of 483’s Issued
4
Warning Letters Issued
0
Countries Inspected
USA
FDA Investigators having one site common
Detailed Analysis
Approach:
Sherry K Markwell prioritizes the specific reporting processes for medical devices, their timeliness and the related record keeping efforts, and seriousness in managing device-related injury reports.
Profile:
FDA investigator Sherry K Markwell has keen attention to the strict regulations set by the FDA centering on Medical Device Reporting (MDR). She pays close attention to the procedural compliance, timeliness and thoroughness of MDR related documentation and reporting. She seems to favor adherence to FDA reporting mandates specifically FDA Form 3500A within required deadlines.
Top Process Types:
Issue Date
Facility Name
Product Type
Form 483
Converted
Warning Letter
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