FDA inspection

Perkinelmer Optoelectronics: FDA inspection ending Oct 21, 2003

FDA inspection 298242 · Voluntary Action Indicated (VAI) · Fremont, CA

Key facts

Inspection ID 298242
Firm Perkinelmer Optoelectronics
FEI number 1000123898
Address 44370 Christy St
City Fremont
State CA
ZIP 94538-3180
Fiscal year 2004
Inspection end date Oct 21, 2003
Classification Voluntary Action Indicated (VAI)
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
  • Yes 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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