Keystone Laboratories, Inc.

Form 483

Memphis, Tennessee, United StatesFEI 1020139Issued February 05, 2016

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 1020139.

Observations3

Issue DateFebruary 05, 2016

StatusNo Warning Letter

Related Inspections8

Establishment Details

Firm: Keystone Laboratories, Inc.
Location: Memphis, Tennessee, United States
FEI Number: 1020139
Product Type: Drugs
Issue Date: February 05, 2016
Country: United States

Inspection History, 2009 to 2017

VAI3

OAI5

VAI means Voluntary 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.

Keystone Laboratories, Inc. FDA Form 483, Memphis, Tennessee, February 5, 2016