FDA Inspection 1041102 — Shire Human Genetic Therapies Inc

Shire Human Genetic Therapies Inc — FEI 3005955297

The FDA completed an inspection of Shire Human Genetic Therapies Inc on Feb 1, 2018 in Cambridge, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 1, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cambridge, MA (United States)

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