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Certified Product Investigation Process (CPIP) - FY10

NOTE: This page is archived for historical purposes and is no longer being maintained or updated.

Current Information can be found at: Certified Product Investigation Process (CPIP) - FY11

Objective

  • Ensure the quality of NIOSH Certified respiratory protective devices used in the field by investigating and resolving non-conformance issues in a timely manner.
  • Respond to all reports of nonconforming respirators.
  • Evaluate corrective actions taken by approval holders to ensure conformance to the criteria listed in 42 CFR, Part 84.

Applicable Standards

  • None

Key Partners

  • NFPA
  • IAFF
  • SEI
  • MSHA
  • OSHA
  • FDA
  • EPA

Stakeholders

  • Respirator Users
  • Enforcement Agencies
  • Emergency Responders
  • Respirator manufacturers - # of new manufacturing codes issued since 2004:
    • Total -79
    • US -32
    • Non -47

Project Scope


  • Communicate and interact with manufacturers and distributors world-wide.
  • Respond to various levels of demand.
  • Establish and enforce accountability for nonconformances.

Milestones

  • None

Outputs

  • 16 on-going CPIP investigations
  • 1 Firefighter reports generated
  • 11 Field investigations completed (non-Firefighter)
  • 2 User notices issued

Outcomes

  • Ensure that NIOSH approved respiratory devices continue to meet or exceed the criteria on which the approval was based.
  • Improved respirator components.
Page last updated: April 5, 2010
Page last reviewed: April 5, 2010
Content Source: National Institute for Occupational Safety and Health (NIOSH)
National Personal Protective Technology Laboratory