Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1000125147.
Observations1
Issue DateApril 16, 2019
StatusNo Warning Letter
Related Inspections5
Establishment Details
Firm
ARMM Inc
Location
Huntington Beach, California, United States
FEI Number
1000125147
Product Type
Devices
Issue Date
April 16, 2019
Country
United States
Inspection History, 2010 to 2020
NAI3
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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