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FDA Inspection
•Medisca Inc•August 3, 2018

Medisca Inc – FDA Inspection, Aug 3, 2018

Record Details

This FDA Inspection record concerns Medisca Inc, with an inspection on August 3, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Medisca Inc
Inspection Date
August 3, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Nayan J. Patel (FDA Associated Person)
View Company Profile

ID · 71ba5e28-ae06-46ca-b520-92b4d6ef3cf9

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1060944
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.25(b)Supervisor Training/Education/Experience

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Medisca Inc

3
DateClassificationOfficeProject area
February 24, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 15, 2016NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
September 14, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Medisca Inc
  • FDA Inspection 982094 - 2016-02-24
  • FDA Inspection 970313 - 2016-01-15
  • FDA Inspection 678687 - 2010-09-14

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