FDA inspection

Nypro FinPack: FDA inspection ending Mar 21, 2014

FDA inspection 871579 · Voluntary Action Indicated (VAI) · Clinton, MA

Key facts

Inspection ID 871579
Firm Nypro FinPack
FEI number 3010665957
Address 25 School St
City Clinton
State MA
ZIP 01510-3419
Fiscal year 2014
Inspection end date Mar 21, 2014
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices
Product type Devices, Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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

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