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FDA inspection

Bell-More Laboratories Inc: FDA inspection ending Apr 23, 2008

FDA inspection 518494 · Voluntary Action Indicated (VAI) · Hampstead, MD

Key facts

Inspection ID 518494
Firm Bell-More Laboratories Inc
FEI number 1150023
Address 4030 Gill Ave
City Hampstead
State MD
ZIP 21074-2213
Fiscal year 2008
Inspection end date Apr 23, 2008
Classification Voluntary Action Indicated (VAI)
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|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug 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Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation
Product type Devices, Drugs

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No 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.

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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