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9960 Maryland Drive, Suite 300 Enrico, Virginia 23233 (804) 3674456 (Tel) (804) 5274472 (Fax) pharmbd@dhp.virginia.gov www.dhp.virginia.gov/pharmacyAPPLICATION FOR A INSPECTION OF FACILITY Check Appropriate
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Start by downloading the re-inspection application form for 10-2020.
02
Carefully read the instructions provided along with the form.
03
Fill out your personal details such as name, address, and contact information in the designated fields.
04
Provide the necessary details about the inspection you are requesting a re-inspection for.
05
Clearly articulate the reasons why you believe a re-inspection is necessary.
06
Attach any supporting documents or evidence that may strengthen your case for a re-inspection.
07
Review the completed application form for any errors or omissions.
08
Submit the filled-out re-inspection application form, along with any required fees, to the appropriate authority or department.
09
Keep a copy of the submitted application and any receipts or confirmation for future reference.
10
Await a response from the authority regarding your re-inspection request.

Who needs re-inspection application 10-2020?

01
Anyone who has undergone an inspection and believes that there were errors, omissions, or unfair assessments made during the initial inspection may need to fill out the re-inspection application 10-2020. This application provides individuals with a formal process to request a re-evaluation of the previous inspection and to address any concerns or discrepancies found.
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Re-inspection application 10 is a form submitted to request a subsequent inspection of a previously inspected item or process.
Any individual or entity responsible for ensuring the compliance and safety of the inspected item or process.
Re-inspection application 10 can typically be filled out online or by submitting a physical form with required information such as contact details, description of item or process, and reason for re-inspection.
The purpose of re-inspection application 10 is to ensure that previously inspected items or processes continue to meet safety and quality standards.
Information such as contact details, description of item or process, previous inspection details, reason for re-inspection, and any relevant documentation.
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