FEI 3007268508

FDA inspection history in Fort Worth, Texas, 2025

1
Form 483

Every document, by year

  • Form 483

2025: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2025One Form 483, at Fort Worth, Texas.

Cited most

Across all site observations on file

  • 21 CFR 1271.55(b)(2)
    What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?
    2
  • 21 CFR 1271.50(a)
    How do I determine whether a donor is eligible?
    1
  • 21 CFR 1271.75(a)(1)
    How do I screen a donor?
    1
  • 21 CFR 1271.90(c)
    Are there other exceptions and what labeling requirements apply?
    1

The complete site file.

All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.

$99

The documents one by one, while the file is prepared

See the documents

Sites

Documents

1 on file, newest first
DateDocumentPrice
2025-04-24483 Form 483$99

Investigators on these documents

Michelle Paxon (1)

FEI number 3007268508 · most recent document Apr 24, 2025

About FEI 3007268508

How many FDA Form 483s has FEI 3007268508 received?

FDA Intel has 1 Form 483 on file for FEI 3007268508; the most recent is dated Apr 24, 2025.

When was FEI 3007268508 last inspected by FDA?

The most recent FDA inspection document on file for FEI 3007268508 is a Form 483 dated Apr 24, 2025, for the site in Fort Worth, Texas.

What did FDA cite at FEI 3007268508?

The regulations cited most in the observations on file for FEI 3007268508 are 21 CFR 1271.55(b)(2) (What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?), 2 times; 21 CFR 1271.50(a) (How do I determine whether a donor is eligible?), 1 time; 21 CFR 1271.75(a)(1) (How do I screen a donor?), 1 time.