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FDA inspection

Abbvie SRL: FDA inspection ending Nov 21, 2017

FDA inspection 1031720 · Voluntary Action Indicated (VAI) · Aprilia

Key facts

Inspection ID 1031720
Firm Abbvie SRL
FEI number 3002806277
Address S.R. 148, Via Pontina 52/S.N.C.
City Aprilia
Fiscal year 2018
Inspection end date Nov 21, 2017
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|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug 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Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug Evaluation|Compliance: Medical Devices|Drug Quality Assurance|New Drug 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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.

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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