FDA inspection

CrestLab, Inc.: FDA inspection ending Apr 28, 2005

FDA inspection 377409 · Official Action Indicated (OAI) · Indianapolis, IN

Key facts

Inspection ID 377409
Firm CrestLab, Inc.
FEI number 1827505
Address 10375 Hague Rd
City Indianapolis
State IN
ZIP 46256-3316
Fiscal year 2005
Inspection end date Apr 28, 2005
Classification Official Action Indicated (OAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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