Elyshia Q. Danaher

FDA investigator

Appears on 3 documents from 2025 to 2026, mostly at sites in Texas. Most often cites what records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain? (21 CFR 1271.55).

3
Documents on file
2.3
Observations per 483
2025
First seen
2026
Most recent

What they cite most

From 7 observations
  • 21 CFR 1271.55
    What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?
    2
  • 21 CFR 606.100
    Standard operating procedures
    2
  • 21 CFR 1271.47
    What procedures must I establish and maintain?
    1
  • 21 CFR 1271.65
    How do I store an HCT/P from a donor determined to be ineligible, and what uses of the HCT/P are not prohibited?
    1
  • 21 CFR 606.160(b)
    Records
    1
  • 21 CFR 630.10(b)
    General donor eligibility requirements
    1

Activity by year

2025: 1, 2026: 2

Where

Texas 2

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Inspection history

3 documents, newest first
FirmOpen
483 Biomat USA IncApr 14, 2026 · Lufkin, Texas
483 Kedplasma LLCMar 3, 2026
483 Center for Assisted Reproduction (CARESep 10, 2025 · Bedford, Texas

About this profile

What does Elyshia Q. Danaher inspect?

Elyshia Q. Danaher appears on 3 documents on file covering 3 sites, mostly in Texas.

What do they cite most often?

21 CFR 1271.55 (what records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?), followed by 21 CFR 606.100 and 21 CFR 1271.47.

Can I read the observations?

Each document page previews the opening words of every observation. The full documents are available to buy, one at a time or together.

How current is this profile?

The most recent document on file for Elyshia Q. Danaher is dated Apr 14, 2026.