Orca1

FDA inspection

Professional Disposables International, Inc.: FDA inspection ending May 28, 2019

FDA inspection 1090866 · Voluntary Action Indicated (VAI) · Orangeburg, NY

Key facts

Inspection ID 1090866
Firm Professional Disposables International, Inc.
FEI number 2411192
Address 2 Nice Pak Park
City Orangeburg
State NY
ZIP 10962-1317
Fiscal year 2019
Inspection end date May 28, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance
Product type Devices, Drugs

At a glance

  • 10–99 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

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