Firm Record

Care-Tech Labs Inc. findings history

80 findings from 4 inspection documents published by regulators. Each row below says what its date means.

US FDA 2024-01-17 ~ 2024-01-17 4 documents 80 findings

Areas cited

Process validationOther quality systemDocumentation and recordsEquipment and facilityLaboratory and QC controlsStability and storageMaterial and supplier controlDeviation, CAPA, and investigationQuality unit oversight

Published inspection documents

2024-01-17 US FDA 23 findingsProcess validation · Equipment and facility · Deviation, CAPA, and investigation · Laboratory and QC controls · Other quality system · Quality unit oversight · Documentation and records · Stability and storage · Material and supplier control There are no written procedures for production and process controls designed to assure that the drug products have the identity, strength, quality, and purity they purport or are represented to possess, Specifically, 2024-01-17 US FDA 19 findingsMaterial and supplier control · Equipment and facility · Other quality system · Quality unit oversight · Laboratory and QC controls · Process validation · Deviation, CAPA, and investigation · Stability and storage · Documentation and records Specific identification tests are not conducted on components that have been accepted based on the supplier's report of analysis. 2024-01-17 US FDA 19 findingsOther quality system · Equipment and facility · Documentation and records · Process validation · Laboratory and QC controls · Stability and storage · Deviation, CAPA, and investigation · Quality unit oversight · Material and supplier control Specificall according to management from approximately 11114/2007 to 212112008 the finn had numerous problems with the HPLC instrumentation. 2024-01-17 US FDA 19 findingsProcess validation · Laboratory and QC controls · Material and supplier control · Equipment and facility · Documentation and records · Stability and storage · Deviation, CAPA, and investigation · Quality unit oversight · Other quality system Written production and process control procedures are not followed in the execution ofproduction and process control functions and documented at the time ofperformance.

About this page

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.

What is included. As of 2026-09-03, only documents that have a detail page (at least 3 findings) are listed. The company may have more documents; the full set is available in Company lookup below.

Companies are grouped by a normalised key, not the displayed name — “… Limited” and “… Ltd.” count as the same company. Translation and classification are automated and may differ in nuance from the source; the basis for judgement is always the regulator's published document.

Full history of Care-Tech Labs Inc. — including inspection classifications Browse by document Go to Findings search