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 3008642652.
Observations7
Issue DateJune 20, 2014
StatusNo Warning Letter
Establishment TypeMedical Device Manufacturer
Related Inspections6
Establishment Details
Firm
Zoll Manufacturing Corp.
Location
Pittsburgh, Pennsylvania, United States
FEI Number
3008642652
Establishment Type
Medical Device Manufacturer
Product Type
Devices
Issue Date
June 20, 2014
Country
United States
Inspection History, 2010 to 2018
NAI3
VAI2
OAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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