Multi-Med, Inc.

Form 483

Keene, New Hampshire, United StatesFEI 1221765Issued July 08, 2010

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 1221765.

Observations9

Issue DateJuly 08, 2010

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Multi-Med, Inc.
Location: Keene, New Hampshire, United States
FEI Number: 1221765
Product Type: Devices
Issue Date: July 08, 2010
Country: United States

Inspection History, 2009 to 2024

NAI3

VAI3

OAI1

NAI means No Action Indicated. 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.

Multi-Med, Inc. FDA Form 483, Keene, New Hampshire, July 8, 2010