Blue Ridge Pharmacy and Compounding Center

FDA inspection history in Raleigh, North Carolina, 2013 to 2016

1
Close-out
1
Form 483

Every document, by year

  • Close-out
  • Form 483

2013: one Form 483; 2016: one close-out letter.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2013One Form 483, at Raleigh, North Carolina.
  2. 2016One close-out letter, at Raleigh, North Carolina.

Cited most

Across all Blue Ridge Pharmacy and Compounding Center observations on file

The complete Blue Ridge Pharmacy and Compounding Center file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2016-06-14Close-out Close-out letter$99
2013-10-23483 Form 483$99

Investigators on these documents

Viviana Matta (1)

FEI number 3014033194 · most recent document Jun 14, 2016

About Blue Ridge Pharmacy and Compounding Center

How many FDA Form 483s has Blue Ridge Pharmacy and Compounding Center received?

FDA Intel has 1 Form 483 on file for Blue Ridge Pharmacy and Compounding Center; the most recent is dated Oct 23, 2013.

When was Blue Ridge Pharmacy and Compounding Center last inspected by FDA?

The most recent FDA inspection document on file for Blue Ridge Pharmacy and Compounding Center is a Form 483 dated Oct 23, 2013, for the site in Raleigh, North Carolina.

What did FDA cite at Blue Ridge Pharmacy and Compounding Center?

The regulations cited most in the observations on file for Blue Ridge Pharmacy and Compounding Center are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.42 (Design and construction features), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time.