Almitech, Inc.

Form 483FOIA Uncovered

Bellmore, New York, United StatesFEI 3005562016Issued March 30, 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 3005562016.

Observations4

Issue DateMarch 30, 2018

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Almitech, Inc.
Location: Bellmore, New York, United States
FEI Number: 3005562016
Product Type: Devices
Issue Date: March 30, 2018
Country: United States

Inspection History, 2009 to 2019

NAI4

OAI1

NAI means No Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Almitech, Inc. FDA Form 483, Bellmore, New York, March 30, 2018