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FDA Inspection
•BEO Pharma Inc•September 18, 2026

BEO Pharma Inc – FDA Inspection, Sep 18, 2026

Record Details

This FDA Inspection record concerns BEO Pharma Inc, with an inspection on September 18, 2026, issued by the Florida District Office, covering human drugs.

Company
BEO Pharma Inc
Inspection Date
September 18, 2026
Product Type
Human Drugs
Office
Florida District Office
People
  • Ashley N. Samuel (Issuing Officer)
  • Saundrea A. Munroe (FDA Associated Person)
View Company Profile

ID · 19e1311a-bde9-484c-9ebd-ff49e147a1b0

Inspection Facts

Inspection number
1337028
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

5
  1. 21 CFR 211.100(a)Absence of Written Procedures
  2. 21 CFR 211.160(b)Scientifically sound laboratory controls
  3. 21 CFR 211.22(d)Procedures not in writing, fully followed
  4. 21 CFR 211.84(b)Representative Samples
  5. 21 CFR 211.89Quarantine of Rejected Components et. al.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of BEO Pharma Inc

1
DateClassificationOfficeProject area
November 4, 2024OAIFlorida District OfficeDrug Quality Assurance
Other documents for BEO Pharma Inc
  • FDA Inspection 1253295 - 2024-11-04

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