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 1000515493.
Observations2
Issue DateApril 12, 2017
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
Remel Inc.
Location
Oakwood Village, Ohio, United States
FEI Number
1000515493
Product Type
Devices
Issue Date
April 12, 2017
Country
United States
Inspection History, 2010 to 2025
NAI1
VAI3
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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