Inspection Record

Vita Pharmacy, LLC dba Talon Pharmacy of Boerne — FDA 483 Findings

US FDAInspected 2020-02-11Published 2020-03-09 6 findingsOther quality systemCleaning validationAseptic processing and sterility assuranceEnvironmental monitoring

View the regulator's official source The source document is always the basis for judgement.

Findings

1Other quality system

In regard to the production of highly potent drugs: A.

2Cleaning validation

On 1/24/20, 1 (Stephen Brown) observed brownish residue on a corner of the HEPA filter located in the ISO 5 workbench area.

3Aseptic processing and sterility assurance

The glass beakers used in the production of sterile, injectable drug products are not depyrogenated prior to use.

4Environmental monitoring

Your firm does not perform environmental monitoring of the <Redacted B4>

5Aseptic processing and sterility assurance

In regard to aseptic practice: A.

6Environmental monitoring

In regard to the latest clean room certification dated 10/3/19: A.

About this record

Extracted automatically from the document US FDA published on 2020-03-09. The source is available at the link above.

This is a record of that moment. Inspection findings are usually followed by the company's response and corrective action, but this page does not know how that turned out. Do not read it as the current state; check the regulator's official announcements for the latest status.

Translation and classification are automated and may differ in nuance from the source.

Other records for this company

Vita Pharmacy, LLC dba Talon Pharmacy of Boerne company profile — full history US FDA documents, 2020 Go to Findings search