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FDA inspection

Syntacoll Gmbh: FDA inspection ending Jun 29, 2018

FDA inspection 1061780 · Voluntary Action Indicated (VAI) · Saal A.D.Donau

Key facts

Inspection ID 1061780
Firm Syntacoll Gmbh
FEI number 3005433617
Address Donaustr. 24
City Saal A.D.Donau
Fiscal year 2018
Inspection end date Jun 29, 2018
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|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New 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Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug Evaluation|Compliance: Medical Devices|New Drug 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Product type Devices, Drugs

At a glance

  • None 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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