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 3006059109.
Observations2
Issue DateFebruary 05, 2026
StatusNo Warning Letter
Establishment TypeMedical Device Manufacturer
Related Inspections6
Establishment Details
Firm
Life Recovery Systems HD, LLC
Location
Kinnelon, New Jersey, United States
FEI Number
3006059109
Establishment Type
Medical Device Manufacturer
Product Type
Devices
Issue Date
February 05, 2026
Country
United States
Inspection History, 2012 to 2026
NAI1
VAI4
OAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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