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 3008778376.
Observations3
Issue DateJuly 10, 2015
StatusNo Warning Letter
Establishment TypeShell Egg Producer
Related Inspections2
Establishment Details
Firm
Lamar Zimmerman
Location
Myerstown, Pennsylvania, United States
FEI Number
3008778376
Establishment Type
Shell Egg Producer
Product Type
Drugs
Issue Date
July 10, 2015
Country
United States
Inspection History, 2011 to 2017
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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