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 3008061617.
Observations2
Issue DateDecember 14, 2017
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
Ambi, Inc
Location
Capitola, California, United States
FEI Number
3008061617
Product Type
Devices
Issue Date
December 14, 2017
Country
United States
Inspection History, 2017 to 2022
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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