Orca1

FDA inspection

Associated Production Services, Inc.: FDA inspection ending Apr 14, 2004

FDA inspection 322935 · No Action Indicated (NAI) · Trevose, PA

Key facts

Inspection ID 322935
Firm Associated Production Services, Inc.
FEI number 2523101
Address 325 Andrews Rd
City Trevose
State PA
ZIP 19053-3429
Fiscal year 2004
Inspection end date Apr 14, 2004
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|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality 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Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological Hazard|Drug Quality Assurance|Foodborne Biological 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Product type Devices, Drugs, Food/Cosmetics

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.

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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