Inspection Record

Shertech Pharmacy, LLC — FDA 483 Findings

US FDAInspected 2019-07-18Published 2019-10-21 4 findingsAseptic processing and sterility assuranceOther quality system

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

Findings

1Aseptic processing and sterility assurance

Personnel engaged in aseptic processing were observed leaving and re-entering the cleanroorn from non-classified areas without first replacing gowning apparel.

2Other quality system

Your firm's records are deficient in that they do not include complete documentation of all data obtained during testing to provide assurances that your product meets release specifications.

3Aseptic processing and sterility assurance

Sporicidal agents were not used in your facility's cleanrooms and/or ISO 5 classified aseptic processing area.

4Aseptic processing and sterility assurance

Personnel touched equipment or other surfaces located outside of the ISO 5 classified aseptic processing area with gloved hands and then engaged in aseptic processing without changing or sanitizing gloves.

About this record

Extracted automatically from the document US FDA published on 2019-10-21. 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

Shertech Pharmacy, LLC company profile — full history US FDA documents, 2019 Go to Findings search