FDA inspection
Synergy Health Daniken AG: FDA inspection ending Sep 27, 2018
FDA inspection 1072629 · No Action Indicated (NAI) · Daniken So
Key facts
| Inspection ID | 1072629 |
|---|---|
| Firm | Synergy Health Daniken AG |
| FEI number | 3002808269 |
| Address | Hogenweidstrasse 6 |
| City | Daniken So |
| Fiscal year | 2018 |
| Inspection end date | Sep 27, 2018 |
| Classification | No Action Indicated (NAI) |
| 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: 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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
- None Citations
- None 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