American Red Cross Biomedical Sevices Headquarters

FDA inspection history in Washington, District of Columbia, 2008

1
Form 483

Every document, by year

  • Form 483

2008: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2008One Form 483, at Washington, District of Columbia.

Cited most

Across all American Red Cross Biomedical Sevices Headquarters observations on file

  • 21 CFR 606.100
    Standard operating procedures
    1
  • 21 CFR 606.171
    Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services
    1

The complete American Red Cross Biomedical Sevices Headquarters 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
2008-07-03483 Form 483$99

Investigators on these documents

Barbara A. Gullick (1)

FEI number 1122335 · most recent document Jul 3, 2008

About American Red Cross Biomedical Sevices Headquarters

How many FDA Form 483s has American Red Cross Biomedical Sevices Headquarters received?

FDA Intel has 1 Form 483 on file for American Red Cross Biomedical Sevices Headquarters; the most recent is dated Jul 3, 2008.

When was American Red Cross Biomedical Sevices Headquarters last inspected by FDA?

The most recent FDA inspection document on file for American Red Cross Biomedical Sevices Headquarters is a Form 483 dated Jul 3, 2008, for the site in Washington, District of Columbia.

What did FDA cite at American Red Cross Biomedical Sevices Headquarters?

The regulations cited most in the observations on file for American Red Cross Biomedical Sevices Headquarters are 21 CFR 606.100 (Standard operating procedures), 1 time; 21 CFR 606.171 (Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services), 1 time.