Home / Inspections / 655409

FDA Inspection 655409 — American Laboratories Pharma, LLC

American Laboratories Pharma, LLC — FEI 1920841

The FDA completed an inspection of American Laboratories Pharma, LLC on March 29, 2010 in Omaha, NE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 29, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Omaha, NE (United States)

Facility

Other inspections at this facility

  • 1237967 (VAI Fri May 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1187283 (OAI Mon Oct 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1037205 (VAI Fri Dec 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 951530 (NAI Fri Sep 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 806926 (NAI Mon Nov 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources