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FDA Inspection
•FORDOZ PHARMA CORPORATION•March 17, 2023

FORDOZ PHARMA CORPORATION – FDA Inspection, Mar 17, 2023

Record Details

This FDA Inspection record concerns FORDOZ PHARMA CORPORATION, with an inspection on March 17, 2023, issued by the New Jersey District Office.

Company
FORDOZ PHARMA CORPORATION
Inspection Date
March 17, 2023
Office
New Jersey District Office
People
  • Alice S. Tsao (FDA Associated Person)
  • Pushpa S. Jayasekara (FDA Associated Person)
View Company Profile

ID · 00df13bf-d33e-4cb4-9e1d-9e893134df59

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1201660
FDA center
Human Drugs
Outcome
Form 483 issued

FDA Citations

4
  1. 21 CFR 211.113(b)Procedures for sterile drug products
  2. 21 CFR 211.142Written warehousing procedures established/followed
  3. 21 CFR 211.42(a)Buildings of Suitable Size, Construction, Location
  4. 21 CFR 211.63Equipment Design, Size and Location

Full citation text and observation details available on the Dashboard.

Other FDA inspections of FORDOZ PHARMA CORPORATION

1
DateClassificationOfficeProject area
November 12, 2025OAINew Jersey District OfficeDrug Quality Assurance
Other documents for FORDOZ PHARMA CORPORATION
  • FDA Inspection 1291050 - 2025-11-12

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