Compliance document

Form FDA 483: Goodwin Biotechnology, Inc.

FDA FOIA

Key facts

Document type Form FDA 483
Firm Goodwin Biotechnology, Inc.
FEI number 3001861303
Inspection 1281924
Collection FDA FOIA

At a glance

  • 10–99 Pages
  • 1–9 FDA inspections at this FEI

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

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The Orca1 document library indexes FDA compliance documents such as Form 483 observations, establishment inspection reports and firm responses. Documents are available to Orca1 subscribers only.

Source: U.S. Food and Drug Administration (FDA) records, Orca1 document library

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