FDA inspection

Cramer Products Inc: FDA inspection ending Jul 17, 2007

FDA inspection 479344 · Voluntary Action Indicated (VAI) · Gardner, KS

Key facts

Inspection ID 479344
Firm Cramer Products Inc
FEI number 1910082
Address 153 W Warren St
City Gardner
State KS
ZIP 66030-1151
Fiscal year 2007
Inspection end date Jul 17, 2007
Classification Voluntary Action Indicated (VAI)
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|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality 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Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Drug Quality Assurance|Food Compos, Stds, 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Product type Devices, Drugs, Food/Cosmetics

At a glance

  • 1–9 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.

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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