Acro Biotech Inc.

Form 483FOIA Uncovered

Rancho Cucamonga, California, United StatesFEI 3005670738Issued May 01, 2018

View FDA's Record for This Firm

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 3005670738.

Observations1

Issue DateMay 01, 2018

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Acro Biotech Inc.
Location: Rancho Cucamonga, California, United States
FEI Number: 3005670738
Product Type: Devices
Issue Date: May 01, 2018
Country: United States

Inspection History, 2013 to 2018

NAI1

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

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Acro Biotech Inc. FDA Form 483, Rancho Cucamonga, California, May 1, 2018