Inspection Record

Dr. Reddy's Laboratories Ltd. — FDA 483 Findings

US FDAInspected 2017-09-15Published 2017-09-26 3 findingsMaterial and supplier controlCleaning validationOther quality system

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

Findings

1Material and supplier control

Manually managed materials in the warehouse are not separated during storage.

2Cleaning validation

Cleaning procedures or clean status is not established.

3Other quality system

Procedures are not established or followed.

About this record

Extracted automatically from the document US FDA published on 2017-09-26. 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

2025-09-05 · US FDA · 4 findings2025-07-18 · US FDA · 6 findings2024-09-16 · Health Canada · 4 findings2023-12-08 · US FDA · 3 findings2023-10-27 · US FDA · 9 findings2023-05-29 · Health Canada · 5 findings
Dr. Reddy's Laboratories Ltd. company profile — full history US FDA documents, 2017 Go to Findings search