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FDA Inspection
•Omega & Delta Co., Inc.•March 20, 2026

Omega & Delta Co., Inc. – FDA Inspection, Mar 20, 2026

Record Details

This FDA Inspection record concerns Omega & Delta Co., Inc., with an inspection on March 20, 2026, issued by the San Juan District Office, covering human drugs.

Company
Omega & Delta Co., Inc.
Inspection Date
March 20, 2026
Product Type
Human Drugs
Office
San Juan District Office
Person
  • Tomika L. Crafter (Investigator)
View Company Profile

ID · 1921469e-8271-4ab4-bad0-ff6b97bad9e1

Inspection Facts

Inspection number
1308236
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 211.100(a)Absence of Written Procedures
  2. 21 CFR 211.180(e)(2)Items to cover on annual reviews

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Omega & Delta Co., Inc.

7
DateClassificationOfficeProject area
October 23, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 6, 2022OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 7, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 16, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 10, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Omega & Delta Co., Inc.
  • FDA Inspection 1221655 - 2023-10-23
  • FDA Inspection 1168919 - 2022-05-06
  • FDA Inspection 1003842 - 2017-02-07
  • FDA Inspection 966974 - 2015-12-16
  • FDA Inspection 859627 - 2013-12-10

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