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483
•Sarasota Medical Products, Inc.•June 12, 2019

Sarasota Medical Products, Inc. – FDA 483, Jun 12, 2019

Record Details

Sarasota Medical Products Inc, a medical device manufacturer in Sarasota, FL, was inspected by the FDA. The inspection revealed significant deficiencies in process validation for sterilization, particularly for HTLA Hydrocolloid adhesive products, as well as inadequate procedures for Medical Device Reporting (MDR). Additionally, device history records were found to be incomplete, indicating a lack of adherence to quality system requirements.

Company
Sarasota Medical Products, Inc.
Inspection date
June 12, 2019
Product type
device
Office
Office of Medical Device and Radiological Health Division II
Person
  • Joshua J. Silvestri
View Company Profile

ID · 4b12fb93-fdde-4a8e-9a93-2b1ee6827eec

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