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OII FOIA Electronic Reading Room

The OII Electronic Reading Room displays copies of select foreign and domestic inspection and related records. We are making these records publicly available either (1) proactively at our discretion or (2) because they are "frequently requested" per the Electronic Freedom of Information Act Amendments of 1996. Some records may be redacted to remove non-public information (see 21 CFR Part 20). For publicly available OII data sets, (such as lists of inspection classifications, 483 observations, etc.), please visit the data sets page. For other OII documents, please visit the OII home page and the FDA Warning Letter page. For other inspection and related records, please search the relevant center reading room page on the main FDA Electronic Reading Room.

FDA is committed to ensuring digital accessibility for people with disabilities. We are continually improving the user experience for everyone and applying the relevant accessibility standards. At the time of initial posting, some records may not be fully accessible to users using assistive technology. If this is the case, a fully accessible version of the record is in preparation and will be posted as soon as it is ready. We regret any inconvenience that this may cause our readers. Please let us know if you encounter accessibility barriers by contacting OII’s Division of Information Disclosure Policy OIIFOIAInquiries@fda.hhs.gov.

To obtain a copy of a record not listed in the OII Reading Room please submit a FOIA request.

Follow the steps outlined on the following webpage to complete an online FOIA request: https://www.accessdata.fda.gov/scripts/foi/FOIRequest/requestinfo.cfm. (Note: As of 3/12/2020, we are asking that all FOIA requests be submitted through our online portal rather than by mail, fax, or courier, to ensure timely logging of the requests.)

Any questions related to FOIA requests may be addressed to the Division of the Freedom of Information Offices at (301) 796-3900. You may also visit the following webpages to learn more about FOIA requests:
https://www.fda.gov/regulatory-information/freedom-information/how-make-foia-request
https://www.accessdata.fda.gov/scripts/foi/FOIRequest/index.cfm.

Content for the ORA FOIA Electronic Reading Room is available on FDA's website for five years before being archived.

To find FOIA archived content for years prior to 2012, visit https://wayback.archive-it.org/7993/20170404012657/https://www.fda.gov/AboutFDA/CentersOffices/OfficeofGlobalRegulatoryOperationsandPolicy/ORA/ORAElectronicReadingRoom/default.htm.

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Record Date Company Name FEI Number Record Type State Country Establishment Type Publish Date Excerpt
US Specialty Formulations LLC 3010680515 483 Pennsylvania Outsourcing Facility
JKR Pharmacy Ventures, LLC 3033262505 483 Kentucky Producer of Sterile and Non Sterile Drug Products
Empower Clinic Services LLC dba Empower Pharma 3011887629 483 Texas Outsourcing Facility
Pure Indulgence Aesthetics 3041017461 483 United States Dispenser of Prescription Drugs
Dr. Reddy’s Laboratories Limited 3009193040 483 India Finished Pharmaceutical Manufacturer
Denver Solutions, LLC 3013438582 483 Colorado Outsourcing Facility
Nubratori, Inc. 3010166491 483 California Outsourcing Facility
Ipca Laboratories Limited 3006057101 483 India API (animal origin) Manufacturer
Delta Pharma Inc 3004034796 483 Mississippi Outsourcing Facility
Pharmathen International S.A. 3009961173 483 Greece Finished Pharmaceutical Manufacturer
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