Piedmont Augusta Transfusion Service FDA Record

Summary

FDA record by year

Piedmont Augusta Transfusion Service's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

7 inspections from Jul 28, 2009 to Aug 7, 2024.

NAI

No objectionable conditions or practices were found during the inspection.

VAI

Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.

OAI

Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Piedmont Augusta Transfusion Service and the FDA: common questions

Has Piedmont Augusta Transfusion Service received an FDA warning letter?

No FDA warning letter addressed to the name "Piedmont Augusta Transfusion Service" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Piedmont Augusta Transfusion Service received an FDA Form 483?

FDA has not published a Form 483 for "Piedmont Augusta Transfusion Service" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Piedmont Augusta Transfusion Service?

The most recent FDA inspection on file ended Aug 7, 2024 at Augusta, GA and was classified NAI. FDA has 7 inspections of Piedmont Augusta Transfusion Service on file.