FDA inspection

FujiFilm Diosynth Biotechnologies U.S.A., Inc.: FDA inspection ending Mar 1, 2019

FDA inspection 1092044 · Voluntary Action Indicated (VAI) · Research Triangle Park, NC

Key facts

Inspection ID 1092044
Firm FujiFilm Diosynth Biotechnologies U.S.A., Inc.
FEI number 3000718852
Address 6051 George Watts Hill Dr
City Research Triangle Park
State NC
ZIP 27709-0218
Fiscal year 2019
Inspection end date Mar 1, 2019
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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