Compliance document

Form FDA 483: KVK Tech, Inc.

FDA FOIA

Key facts

Document type Form FDA 483
Firm KVK Tech, Inc.
FEI number 3005117563
Inspection 1175552
Collection FDA FOIA

At a glance

  • 10–99 Pages
  • 10–99 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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Source: U.S. Food and Drug Administration (FDA) records, Orca1 document library

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