FDA inspection

Analytical Biochemistry Laboratories Inc. dba ABC Labs. Inc.: FDA inspection ending Jul 31, 2008

FDA inspection 529706 · No Action Indicated (NAI) · Columbia, MO

Key facts

Inspection ID 529706
Firm Analytical Biochemistry Laboratories Inc. dba ABC Labs. Inc.
FEI number 1925415
Address 7200 E Abc Ln
City Columbia
State MO
ZIP 65202-8807
Fiscal year 2008
Inspection end date Jul 31, 2008
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug 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Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug 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Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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