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FDA Inspection
•Chamindra Laverty•January 14, 2026

FDA Inspection 1298982 - Chamindra Laverty - January 14, 2026

Record Details

This FDA Inspection record concerns Chamindra Laverty, with an inspection on January 14, 2026, issued by the Los Angeles District Office, covering human drugs.

Company
Chamindra Laverty
Inspection Date
January 14, 2026
Product Type
Human Drugs
Office
Los Angeles District Office
Person
  • Raman K. Kaushal (Issuing Officer)
View Company Profile

ID · 0fab053b-e8ea-4881-a837-dba917773ced

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1298982
FDA center
Human Drugs
Project area
Bioresearch Monitoring: Human Drugs
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. 21 CFR 312.60FD-1572, protocol compliance

Full citation text and observation details available on the Dashboard.

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