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•United States

LasikPlus, Louisville, KY – FDA Inspections

Inspection records and compliance data for LasikPlus in Louisville, Kentucky. 1 FDA inspection on record (1 OAI), last inspected July 14, 2009.

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Company Profile

This profile covers LasikPlus based in Louisville, Kentucky, United States.

FDA Inspection History

FDA inspections
1
OAI
1
VAI
0
NAI
0
Form 483s
0
Warning letters
0

Inspected July 14, 2009.

Most cited issue areas

  • Adverse events--all info not in file1 inspection
  • Failure to Submit Annual Reports1 inspection
  • Lack of System for Event Evaluations1 inspection

FDA inspections (1)

DateResultFDA center(s)Insp. #
July 14, 2009OAIMedical Devices & Rad Health · Compliance: Devices596008
FDA documents

No Form 483s, Warning Letters or EIRs on record.

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Medshare, Inc.
Philip A TIbbs MD
Kentucky Clinical Trials Laboratory
Ryan J. Krupp, M.D., Clinical Investigator
Wicked Technologies
Alexander G Digenis MD
Company Information

Name

LasikPlus

FEI Number

3007694927

Address

3999 Dutchmans Ln Ste 5f, Louisville, Kentucky 40207, United States

Country

United States

ID: 6b69adc9-14b6-4c90-9d07-c21b6b52df37

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