Sciarra Laboratories, Inc.

Form 483

Hicksville, New York, United StatesFEI 1000306996Issued June 03, 2011

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 1000306996.

Observations2

Issue DateJune 03, 2011

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Sciarra Laboratories, Inc.
Location: Hicksville, New York, United States
FEI Number: 1000306996
Product Type: Devices
Issue Date: June 03, 2011
Country: United States

Inspection History, 2010 to 2023

NAI8

VAI2

NAI means No Action Indicated. VAI means Voluntary 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.

Sciarra Laboratories, Inc. FDA Form 483, Hicksville, New York, June 3, 2011