FDA inspection

Honeywell Safety Products USA, Inc.: FDA inspection ending Dec 10, 2018

FDA inspection 1082633 · No Action Indicated (NAI) · San Diego, CA

Key facts

Inspection ID 1082633
Firm Honeywell Safety Products USA, Inc.
FEI number 3010588332
Address 7828 Waterville Rd
City San Diego
State CA
ZIP 92154
Country United States
Fiscal year 2019
Inspection end date Dec 10, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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