FDA inspection

Roberts Oxygen Company Inc: FDA inspection ending Oct 24, 2002

FDA inspection 245490 · Voluntary Action Indicated (VAI) · Gaithersburg, MD

Key facts

Inspection ID 245490
Firm Roberts Oxygen Company Inc
FEI number 1150053
Address 17011 Railroad St
City Gaithersburg
State MD
ZIP 20877-4230
Fiscal year 2003
Inspection end date Oct 24, 2002
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|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality 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&Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal 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Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev
Product type Devices, Drugs

At a glance

  • 1–9 Citations
  • 1–9 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.

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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