Benjamin D. Moncarz Chief Financial Officer - FDA | Official Website
Benjamin D. Moncarz Chief Financial Officer - FDA | Official Website
This is a 64.3% decrease from the number of companies cited in the previous year.
Of the 21 citations issued, the most common citation was 'Procedures for corrective and preventive action have not been adequately established'.
Most of the companies cited were involved in the Devices sector. The second most common type of company cited in the time period worked in the the Food and Cosmetics sector.
All of the companies cited should take voluntary actions to correct their managing operations.
The FDA routinely inspects facilities across the nation to determine if the workplace and their products are compliant with FDA-regulated laws and regulations implemented to improve overall public health. Inspection results are then disclosed publicly.
The FDA is a government agency that is primarily responsible for monitoring the production and distribution of human and animal drugs, biological products, medical supplies and tobacco products for safety quality, according to its website.
Company Name | Area of Business | Inspection Date | Issue Cited |
---|---|---|---|
Fresenius Kabi USA, LLC | Drugs | 10/13/2023 | Procedures for sterile drug products |
Fresenius Kabi USA, LLC | Drugs | 10/13/2023 | Investigations of discrepancies, failures |
Fresenius Kabi USA, LLC | Devices | 08/30/2023 | Lack of or inadequate procedures |
Fruit Fresh Up, Inc. | Food and Cosmetics | 03/20/2023 | Equipment and utensils - Design and maintenance |
Fruit Fresh Up, Inc. | Food and Cosmetics | 03/20/2023 | Process preventive controls - Appropriate (Adequate) |
Fruit Fresh Up, Inc. | Food and Cosmetics | 03/20/2023 | Sanitation preventive controls - Appropriate (Adequate) |
Nyumbani Hakuna Matata, LLC | Food and Cosmetics | 08/24/2023 | Importer verification |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Label to bear a unique device identifier |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Training records |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Purchasing controls, Lack of or inadequate procedures |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Process control procedures, Lack of or inadequate procedures |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Software validation for automated processes |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Incoming acceptance records, documentation |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Lack of or inadequate procedures |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | DHR content |
Orthodent Laboratory, Inc. | Devices | 11/13/2023 | Devices subject to device identification GUDID data submission requirements. |
You First Services, Inc. | Devices | 12/18/2023 | Label to bear a unique device identifier |
You First Services, Inc. | Devices | 12/18/2023 | Training records |
You First Services, Inc. | Devices | 12/18/2023 | Lack of or inadequate procedures |
You First Services, Inc. | Devices | 12/18/2023 | Lack of or inadequate complaint procedures |
You First Services, Inc. | Devices | 12/18/2023 | Devices subject to device identification GUDID data submission requirements. |