FDA inspection

Hayward Laboratories, Inc.: FDA inspection ending Jul 20, 2017

FDA inspection 1019019 · Voluntary Action Indicated (VAI) · E Stroudsburg, PA

Key facts

Inspection ID 1019019
Firm Hayward Laboratories, Inc.
FEI number 2220345
Address 1921 Paradise Trl
City E Stroudsburg
State PA
ZIP 18301
Country United States
Fiscal year 2017
Inspection end date Jul 20, 2017
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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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