FDA Intel

Variamed, LLC

FDA inspection history in Chattanooga, Tennessee, 2024

1
Form 483

Every document, by year

  • Form 483

2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2024One Form 483, at Chattanooga, Tennessee.

Cited most

Across all Variamed observations on file

  • 21 CFR 820
    1
  • 21 CFR 830
    1
  • 21 CFR 801.20(a)
    Label to bear a unique device identifier
    1
  • 21 CFR 803.17
    What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?
    1
  • 21 CFR 820.100(a)
    Corrective and preventive action
    1

The complete Variamed 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
2024-12-18483 Form 483$99

Investigators on these documents

Jamie P. Webb (1)Lashawn M. Elam (1)

FEI number 3010405322 · most recent document Dec 18, 2024

About Variamed, LLC

How many FDA Form 483s has Variamed, LLC received?

FDA Intel has 1 Form 483 on file for Variamed, LLC; the most recent is dated Dec 18, 2024.

When was Variamed, LLC last inspected by FDA?

The most recent FDA inspection document on file for Variamed, LLC is a Form 483 dated Dec 18, 2024, for the site in Chattanooga, Tennessee.

What did FDA cite at Variamed, LLC?

The regulations cited most in the observations on file for Variamed, LLC are 21 CFR 820, 1 time; 21 CFR 830, 1 time; 21 CFR 801.20(a) (Label to bear a unique device identifier), 1 time.