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FDA Inspection
•DeVere Company, Inc.•June 4, 2025

DeVere Company, Inc. – FDA Inspection, Jun 4, 2025

Record Details

This FDA Inspection record concerns DeVere Company, Inc., with an inspection on June 4, 2025, issued by the Minneapolis District Office, covering human drugs.

Company
DeVere Company, Inc.
Inspection Date
June 4, 2025
Product Type
Human Drugs
Office
Minneapolis District Office
Person
  • Ucheabuchi C. Chudi-Nwankwor (FDA Associated Person)
View Company Profile

ID · 820b2885-a281-4da2-a581-96763d20f2c1

Inspection Facts

Inspection number
1272054
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

FDA Citations

9
  1. 21 CFR 211.100(a)Absence of Written Procedures
  2. 21 CFR 211.160(b)Scientifically sound laboratory controls
  3. 21 CFR 211.165(e)Test methods
  4. 21 CFR 211.166(a)Written program not followed
  5. 21 CFR 211.188(b)Batch production and Batch Control Record Requirements
  6. 21 CFR 211.192Investigations of discrepancies, failures
  7. 21 CFR 211.22(d)Procedures not in writing, fully followed
  8. 21 CFR 211.84(d)(2)Component identification test
  9. 21 CFR 211.84(d)(2)Establish reliability of supplier's C of A

Full citation text and observation details available on the Dashboard.

Other FDA inspections of DeVere Company, Inc.

1
DateClassificationOfficeProject area
February 2, 2018VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for DeVere Company, Inc.
  • FDA Inspection 1040102 - 2018-02-02

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