Orca1

FDA inspection

Cilag AG: FDA inspection ending May 19, 2017

FDA inspection 1014940 · Voluntary Action Indicated (VAI) · Schaffhausen

Key facts

Inspection ID 1014940
Firm Cilag AG
FEI number 3002806695
Address Hochstrasse 201
City Schaffhausen
Fiscal year 2017
Inspection end date May 19, 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|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance
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
  • 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

Browse all FDA inspections