Repro-Med Systems, Inc.

Form 483

Chester, New York, United StatesFEI 1318360Issued May 22, 2017

View Form 483 PDF

Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1318360.

Observations8

Issue DateMay 22, 2017

StatusNo Warning Letter

Establishment TypeMedical Device Manufacturer

Related Inspections6

Establishment Details

Firm: Repro-Med Systems, Inc.
Location: Chester, New York, United States
FEI Number: 1318360
Establishment Type: Medical Device Manufacturer
Product Type: Devices
Issue Date: May 22, 2017
Country: United States

Inspection History, 2009 to 2017

NAI2

VAI3

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Repro-Med Systems, Inc. FDA Form 483, Chester, New York, May 22, 2017