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483
•Valgene Incorporated dba Cape Drugs•December 2, 2021

Valgene Incorporated dba Cape Drugs – FDA 483, Dec 2, 2021

Record Details

An FDA inspection of Valgene Incorporated dba Cape Drugs in Annapolis, MD, a producer of sterile and non-sterile drug products, revealed significant deficiencies in aseptic processing and facility controls. Observations included insufficient disinfectant contact time, difficult-to-clean surfaces with exposed particle-generating materials, and facility design flaws allowing poor quality air into classified areas. Additionally, ISO 5 classified areas were not properly certified under dynamic conditions, indicating a high risk to sterile product quality.

Company
Valgene Incorporated dba Cape Drugs
Inspection date
December 2, 2021
Product type
drugs
Office
Office of Regulatory Affairs
People
  • Sena G. Dissmeyer
  • Kathleen M. Jordan
View Company Profile

ID · 8ceb6ae5-e71f-4733-befc-d2f765413f94

Violation Codes5
21 CFR 211.46(b)21 CFR 211.4221 CFR 211.42(c)(10)21 CFR 211.4421 CFR 211.42(c)(11)

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Other documents for Valgene Incorporated dba Cape Drugs
  • UNTITLED_LETTER - 2022-11-03November 3, 2022
  • 483 - 2018-01-22January 22, 2018
  • 483 - 2015-10-07October 7, 2015

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