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FDA Inspection 1022355 — Bioserv Corporation

Bioserv Corporation — FEI 2027352

The FDA completed an inspection of Bioserv Corporation on July 31, 2017 in San Diego, 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
July 31, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)

Facility

Other inspections at this facility

  • 1195989 (NAI Thu Jan 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 863803 (NAI Thu Jan 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 804269 (NAI Wed Oct 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 756094 (VAI Wed Dec 07 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 656899 (NAI Mon Apr 12 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources