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483
•Wise Pharmacy•June 21, 2019

Wise Pharmacy – FDA 483, Jun 21, 2019

Record Details

An FDA inspection of Joe Wise Pharmacy, Inc. DBA Wise Pharmacy in Littleton, CO, a producer of sterile and non-sterile drug products, revealed significant deficiencies in aseptic processing, hazardous drug handling, and environmental controls. Repeat observations from a previous inspection highlighted issues with the classification of aseptic areas and the presence of sinks in cleanrooms. The firm also failed to use pharmaceutical grade water and adequately monitor its aseptic processing environment.

Company
Wise Pharmacy
Inspection date
June 21, 2019
Product type
drugs
Office
Denver District Office
Person
  • Jamie L. C. Dion
View Company Profile

ID · a7a02aa3-2727-422e-8be3-c8ad42fd3d47

Violation Codes3
FD&C Act 801(a)(3)21 CFR 331(c)21 U.S.C. 324(a)(4)

Full citation text and observation details available on the Dashboard.

Other documents for Wise Pharmacy
  • 483 - 2017-05-23May 23, 2017

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