Home / Inspections / 749646

FDA Inspection 749646 — Allermed Laboratories, Inc.

Allermed Laboratories, Inc. — FEI 1000098920

The FDA completed an inspection of Allermed Laboratories, Inc. on September 27, 2011 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 27, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
San Diego, CA (United States)

Facility

Other inspections at this facility

  • 1228221 (VAI Wed Jan 31 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1071500 (VAI Mon Nov 12 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022877 (VAI Wed Jun 14 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933388 (VAI Mon Jul 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 843070 (VAI Mon Aug 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources