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483
•Dermazone LLC•April 11, 2019

Dermazone LLC – FDA 483, Apr 11, 2019

Record Details

Perrazone Solutions, Inc., a medical device contract manufacturer in Saint Petersburg, FL, received a Form FDA 483 following an inspection from April 8-11, 2019. The inspection revealed significant deficiencies in the firm's quality system, including inadequate procedures for change control, process control, calibration, and personnel training. These observations indicate a need for improved adherence to regulatory requirements for medical device manufacturing.

Company
Dermazone LLC
Inspection date
April 11, 2019
Product type
device
Office
Office of Medical Device and Radiological Health Division II
Person
  • Stanley B. Eugene (investigator)
View Company Profile

ID · 0dfb36de-04ff-4036-a0fe-683d4018d87b

Other documents for Dermazone LLC
  • 483 - 2022-12-06December 6, 2022

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