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FDA Inspection 667874 — Rapid Diagnostics, Division Of Mp Biomedicals, Llc

Rapid Diagnostics, Division Of Mp Biomedicals, Llc — FEI 3002680320

The FDA completed an inspection of Rapid Diagnostics, Division Of Mp Biomedicals, Llc on June 17, 2010 in Burlingame, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 17, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Burlingame, CA (United States)

Facility

Other inspections at this facility

  • 968191 (NAI Thu Feb 04 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 916288 (OAI Mon Mar 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 782534 (OAI Mon May 14 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources