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FDA Inspection
•Srdan Verstovsek•August 11, 2017

Srdan Verstovsek – FDA Inspection, Aug 11, 2017

Record Details

This FDA Inspection record concerns Srdan Verstovsek, with an inspection on August 11, 2017, issued by the Dallas District Office, covering human drugs.

Company
Srdan Verstovsek
Inspection Date
August 11, 2017
Product Type
Human Drugs
Office
Dallas District Office
People
  • Leighton K. Ngai (Company Rep)
  • Rachel M. Skeete (Issuing Officer)
View Company Profile

ID · ce84275b-3a2c-44f3-91a9-20bb57f3f64e

Inspection Facts

Inspection number
1021218
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

4
  1. 21 CFR 312.60FD-1572, protocol compliance
  2. 21 CFR 312.60Informed consent
  3. 21 CFR 312.62(a)Accountability records
  4. 21 CFR 312.62(b)Case history records- inadequate or inadequate

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Srdan Verstovsek

1
DateClassificationOfficeProject area
September 18, 2014NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Srdan Verstovsek
  • FDA Inspection 902563 - 2014-09-18

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