Orca1

FDA inspection

Microbiological Consultants, Inc.: FDA inspection ending Mar 11, 2011

FDA inspection 718131 · No Action Indicated (NAI) · Huntington, WV

Key facts

Inspection ID 718131
Firm Microbiological Consultants, Inc.
FEI number 1120998
Address 617 9th Ave
City Huntington
State WV
ZIP 25701-2716
Fiscal year 2011
Inspection end date Mar 11, 2011
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation
Product type Devices, Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

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

Other inspections at this establishment

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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