FDA Inspection 969065 — Life Recovery Systems HD, LLC

Life Recovery Systems HD, LLC — FEI 3006059109

The FDA completed an inspection of Life Recovery Systems HD, LLC on March 14, 2016 in Kinnelon, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 14, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kinnelon, NJ (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
342521 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.