Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.

Form 483

Saint Louis, Missouri, United StatesFEI 1950222Issued November 25, 2014

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1950222.

Observations13

Issue DateNovember 25, 2014

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
Location: Saint Louis, Missouri, United States
FEI Number: 1950222
Product Type: Devices
Issue Date: November 25, 2014
Country: United States

Inspection History, 2013 to 2026

VAI3

OAI7

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. FDA Form 483, Saint Louis, Missouri, November 25, 2014