FDA inspection

Synergy Health AST, LLC: FDA inspection ending Jun 6, 2006

FDA inspection 432414 · No Action Indicated (NAI) · San Diego, CA

Key facts

Inspection ID 432414
Firm Synergy Health AST, LLC
FEI number 1000518731
Address 9020 Activity Rd Ste D
City San Diego
State CA
ZIP 92126-4454
Fiscal year 2006
Inspection end date Jun 6, 2006
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|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med 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Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices
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
  • 10–99 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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