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 3004504906.
Observations10
Issue DateAugust 05, 2015
StatusNo Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections3
Establishment Details
Firm
Techni Med, Inc. dba The Compounder
Location
Aurora, Illinois, United States
FEI Number
3004504906
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
August 05, 2015
Country
United States
Inspection History, 2015 to 2019
VAI1
OAI2
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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